--- title: "Bard Access Systems, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Bard Access Systems, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/bard-access-systems-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Bard Access Systems, Inc. recall records **19** reported ongoing 19 records in this archive. Latest source date Aug 10, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 10, 2026 FDA device enforcement ### [Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; Power-Trialysis Short-Term Straight Dia...](https://isitonrecall.com/recall/fda-device-z-2984-2026-power-trialysis-short-term-straight-dialysis-catheter-ref-5605150-power-trialysis-short-term-straigh/) this is a downstream recall of class I recall RES 98777 Class I Reported ongoing Distribution: US: FL, IL, OH, VA, MD, TX, WI, GA, TN, IN, SC, NC, MI, PA, OR, OK, AZ, MS, NJ, AL, CA, CO, MA, NV, ID, MO, LA, WA, KY, IA, NH, NY, KS, HI, NE, MN, MT, WY, AR, RI, WV, UT, PR, D... [Official source for Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term S...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2984-2026%22) Aug 10, 2026 FDA device enforcement ### [DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625200; DuoGlide Short-Term Straight Dialysis Catheter, REF: ...](https://isitonrecall.com/recall/fda-device-z-2985-2026-duoglide-short-term-straight-dialysis-catheter-ref-5625150-duoglide-short-term-straight-dialysis-cat/) this is a downstream recall of class I recall RES 98777 Class I Reported ongoing Distribution: US: FL, IL, OH, VA, MD, TX, WI, GA, TN, IN, SC, NC, MI, PA, OR, OK, AZ, MS, NJ, AL, CA, CO, MA, NV, ID, MO, LA, WA, KY, IA, NH, NY, KS, HI, NE, MN, MT, WY, AR, RI, WV, UT, PR, D... [Official source for DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialys...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2985-2026%22) Jul 30, 2026 FDA device enforcement ### [BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF: D015251NK, BD Needle Kit for Powered Driver 35mm x 15Ga, REF: D0...](https://isitonrecall.com/recall/fda-device-z-2872-2026-bd-needle-kit-for-powered-driver-15mm-x-15ga-ref-d015151nk-bd-needle-kit-for-powered-driver-25mm-x-1/) After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the ne... Class I Reported ongoing Distribution: US: MA, FL, IA, SC, IL, NY, UT, NJ, ID, IN, PA, CA, TX, OH, MO, VA, MD, NC, AL, MN, CO, KY, LA, NV, OK, MS, AZ, MI, GA, AR, KS, TN. OUS: CA, SG [Official source for BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2872-2026%22) May 21, 2026 FDA device enforcement ### [OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI Code: 0110885403108365 TPT1000 THORACENTESIS/PARACENTESIS ...](https://isitonrecall.com/recall/fda-device-z-2655-2026-otp5000-thora-para-tray-5fr-non-valved-udi-di-code-0110885403284748-pig1260t-safe-t-centesis-tray-6f/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS T...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2655-2026%22) May 21, 2026 FDA device enforcement ### [CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline ...](https://isitonrecall.com/recall/fda-device-z-2656-2026-ck000495a-poly-midline-catheter-4-fr-single-lumen-udi-di-code-00801741121609-ck000566-poly-midline-c/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midli...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2656-2026%22) May 21, 2026 FDA device enforcement ### [5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The intended use of the Short-Term Dialysis Catheter is attaining temporary/s...](https://isitonrecall.com/recall/fda-device-z-2657-2026-5625240-duoglide-short-term-straight-dialysis-catheter-13-fr-dual-lumen-udi-di-code-00801741042119-t/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 008017410421...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2657-2026%22) May 21, 2026 FDA device enforcement ### [CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide internal reinforcement to aid in catheter placement.](https://isitonrecall.com/recall/fda-device-z-2658-2026-ck000662-powerpicc-solo-hf-catheter-5-fr-triple-lumen-udi-di-code-00801741129674-catheter-stylets-pr/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylet...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2658-2026%22) May 21, 2026 FDA device enforcement ### [1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC SV Catheter 3 Fr Single-Lumen REKV2227 00801741027536 The PowerPlCC SV catheters are in...](https://isitonrecall.com/recall/fda-device-z-2659-2026-1274108d-powerpicc-sv-catheter-4-fr-dual-lumen-rekw2449-00801741087110-3173108d-powerpicc-sv-cathete/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC SV Cath...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2659-2026%22) May 21, 2026 FDA device enforcement ### [5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr ...](https://isitonrecall.com/recall/fda-device-z-2660-2026-5605150-power-trialysis-short-term-straight-dialysis-catheter-13-fr-triple-lumen-udi-di-code-0080174/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 008...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2660-2026%22) May 21, 2026 FDA device enforcement ### [5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107177 5855300 Power-Trialysis Slim-Cath Straight Short-Term Dial...](https://isitonrecall.com/recall/fda-device-z-2661-2026-5855240-power-trialysis-slim-cath-straight-short-term-dialysis-catheter-12-fr-triple-lumen-udi-di-co/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2661-2026%22) May 21, 2026 FDA device enforcement ### [CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138713 P4153108D PowerMidline ...](https://isitonrecall.com/recall/fda-device-z-2662-2026-ck000727-powermidline-catheter-4-fr-single-lumen-udi-di-code-00801741138478-ck000729-powermidline-ca/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729 PowerMidlin...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2662-2026%22) May 21, 2026 FDA device enforcement ### [CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129278 P4254108D PowerMidline Cat...](https://isitonrecall.com/recall/fda-device-z-2663-2026-ck000980a-powermidline-catheter-4-fr-dual-lumen-udi-di-code-00801741236150-p4254108-powermidline-cat/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2663-2026%22) May 21, 2026 FDA device enforcement ### [CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 CK000883 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188800 CK000884A P...](https://isitonrecall.com/recall/fda-device-z-2664-2026-ck000525b-powerpicc-provena-solo-catheter-4-fr-dual-lumen-udi-di-code-00801741236129-ck000883-powerp/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 CK000883 Po...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2664-2026%22) May 21, 2026 FDA device enforcement ### [7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 The Groshong¿ NXT PICC provides short (less than 30 days) or long (greater than 30 days) ter...](https://isitonrecall.com/recall/fda-device-z-2665-2026-7617408-groshong-nxt-clearvue-catheter-4-fr-single-lumen-udi-di-code-00801741035258-the-groshong-nxt/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 The Groshong...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2665-2026%22) May 21, 2026 FDA device enforcement ### [1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034602 1174108D3 PowerPICC Catheter...](https://isitonrecall.com/recall/fda-device-z-2666-2026-1174108-powerpicc-catheter-4-fr-single-lumen-udi-di-code-00801741154935-1295108-powerpicc-solo-cathe/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO C...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2666-2026%22) May 21, 2026 FDA device enforcement ### [CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154003 S4153108BP Prove...](https://isitonrecall.com/recall/fda-device-z-2667-2026-ck000880-provena-midline-catheter-4-fr-dual-lumen-udi-di-code-00801741188770-s4153108bdp-provena-mid/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Provena...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2667-2026%22) May 21, 2026 FDA device enforcement ### [4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108501 The Soft Tissue Biopsy devices are indicated for u...](https://isitonrecall.com/recall/fda-device-z-2668-2026-4380-economy-soft-tissue-biopsy-tray-udi-di-code-0110885403108563-4382a-soft-tissue-biopsy-tray-udi/) Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Class II Reported ongoing Distribution: Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC,... [Official source for 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE BIOPSY TRAY ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2668-2026%22) Mar 11, 2025 FDA device enforcement ### [BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118, CK000955, 3174135, CK000617, CK000839, 3194355, 6174118...](https://isitonrecall.com/recall/fda-device-z-1507-2025-bd-4-fr-single-lumen-powerpicc-catheters-ref-3174155-ck000540-3174118-ck000483-3174335-3174355-ck000/) Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfor... Class I Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of WI, NC, TX, NY, CA, MN, MT, RI, MA, OH, CT, SC, IL, CO, VA, NJ, GA, UT, FL, PA, IN, MD, KY, AZ, MI, WA, HI, MO,... [Official source for BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 317...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1507-2025%22) Jun 20, 2022 FDA device enforcement ### [Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/ BD Manual Driver Needle Kit 15mm x 15Ga, D015251NK/ BD Ne...](https://isitonrecall.com/recall/fda-device-z-1397-2022-intraosseous-needle-and-driver-catalog-device-name-d015151nk-bd-needle-kit-for-powered-driver-15mm-x/) BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss of intraosseous access; 2) Stylet safety mechanism may not engage as... Class I Reported ongoing Distribution: Distribution US nationwide and Canada. [Official source for Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1397-2022%22) ## Reasons in these listed records - this is a downstream recall of class I recall RES 98777 - After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out... - Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. - Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleedi... These examples come from this result page and are not a ranking of every recall reason. ## Checking Bard Access Systems, Inc. ### Is there a recall on bard access systems, inc. right now? This archive contains 19 records, including 19 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Bard Access Systems, Inc.](https://isitonrecall.com/check/?q=Bard%20Access%20Systems%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)