--- title: "Bard Peripheral Vascular Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Bard Peripheral Vascular 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-peripheral-vascular-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Bard Peripheral Vascular Inc recall records **27** reported ongoing 27 records in this archive. Latest source date Dec 12, 2025. 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 Dec 12, 2025 FDA device enforcement ### [Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060](https://isitonrecall.com/recall/fda-device-z-1367-2026-broviac-4-2-fr-single-lumen-cv-catheter-cutdown-tray-with-surecuff-tissue-ingrowth-cuff-cat-60060/) Due to damage to outer tray that can potentially compromise the sterile barrier Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of 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, N... [Official source for Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1367-2026%22) Nov 6, 2025 FDA device enforcement ### [Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,](https://isitonrecall.com/recall/fda-device-z-0887-2026-safe-t-centesis-6-fr-catheter-drainage-tray-ref-pig1260t/) Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believ... Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, MN, IN, MI, LA. [Official source for Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0887-2026%22) Aug 21, 2025 FDA device enforcement ### [Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the Venclose EVSRF Ablation Catheter prior to use. The Venclose di...](https://isitonrecall.com/recall/fda-device-z-2638-2025-venclose-digirf-generators-model-vcrfg1-with-software-3-35-designed-to-identify-internal-wiring-anom/) Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is exec... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of NJ, NY, FL, LA, VA, CA, TX, NV, PA, NE, TN, IL, AZ, SC, AK, GA, CO, HI, OH, NC, WI, WV, MD, MO, AL, OK, MS, PR,... [Official source for Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2638-2025%22) Feb 5, 2025 FDA device enforcement ### [Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239](https://isitonrecall.com/recall/fda-device-z-1244-2025-rotarex-atherectomy-system-and-instructions-for-use-bd-set-rotarex-s-6-f-x-110-cm-ref-80236-s-6-f-x/) Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require r... Class I Reported ongoing Distribution: US Nationwide Distribution: NY, VA, KY, IN, OR, FL, MD, NJ, LA, CO, PR, PA, MS, MI, TX, KS, IL, CA, GA, OH, AL, NC, ND, AZ, SC, TN, UT, AR, WI, SD, MA, MO, ME, DE, WV , NV, NH, ... [Official source for Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1244-2025%22) Sep 30, 2024 FDA device enforcement ### [Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10 CM, REF: MQ1210; BARD MARQUEE Kit 12G X 13 CM, REF: MQK1213...](https://isitonrecall.com/recall/fda-device-z-0467-2025-bard-marquee-disposable-core-biopsy-instrument-kit-bard-marquee-kit-12g-x-10-cm-ref-mqk1210-bard-mar/) Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle detachment and misplacement, which could le... Class II Reported ongoing Distribution: Worldwide - US Nationwide including in the states of WA, LA, MN, PA, UT, SC, OK, KY, AZ, IL, TX, NJ, NY, FL, TN, IN, OH, NC, CO, VA, GA, MD, CA, AL, WI, MO, IA, CT, NE, MI, MS, ... [Official source for Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; B...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0467-2025%22) Sep 4, 2024 FDA device enforcement ### [The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a procedure in which a refluxing vein is thermally coagulated to pe...](https://isitonrecall.com/recall/fda-device-z-0371-2025-the-evsrf-catheter-is-a-sterile-single-use-disposable-medical-device-for-endovenous-radiofrequency-a/) The Venclose" RF Ablation Catheters may have been manufactured with internal wiring error. The red and yellow signal wires were soldered on swapped ports of the catheter PCB. This error in wire configuration would lead to power being applied through the pro... Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, N... [Official source for The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequen...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0371-2025%22) Aug 2, 2024 FDA device enforcement ### [BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy System (instrument and needles) is intended for use in obtaini...](https://isitonrecall.com/recall/fda-device-z-3206-2024-bard-magnum-disposable-core-tissue-biopsy-needle-ref-mn1410-mn-1420-mn1610-mn1616-mn1820-mn2010-the/) Due to possible packaging damage (indentations/cuts) cause by manufacturing process. As a result of the packaging damage, may cause the sterile barrier to be compromised. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the Puerto Rico and the countries of Canada, Pakistan, Peru, India, Malaysia, China, Brazil, Mexico, Japan, Chile, Australia. [Official source for BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3206-2024%22) Jul 10, 2024 FDA device enforcement ### [Guidewire 70cm x 1mm (0.038 ) REF 5583705 These accessories are intended for use with Bard 14.5 Fr. Long-Term Dual Lumen Hemodialysis Catheters. Please refer to the applicable c...](https://isitonrecall.com/recall/fda-device-z-3062-2024-guidewire-70cm-x-1mm-0-038-ref-5583705-these-accessories-are-intended-for-use-with-bard-14-5-fr-long/) Due to guidewires being manufactured incorrectly with the guidewires being mis-assembled within the hoop such that the proximal (stiff) end of the guidewire is located at the distal end of the hoop. Injury could occur if the user attempts to insert the prox... Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of OH, TX, and WV. The countries of Belgium, Canada, France, Italy, and United Kingdom. [Official source for Guidewire 70cm x 1mm (0.038 ) REF 5583705 These accessories are intended for use with Bard 14.5 F...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3062-2024%22) Nov 14, 2023 FDA device enforcement ### [BD Recanalization System, REF: BDRECANSYSTEM](https://isitonrecall.com/recall/fda-device-z-0676-2024-bd-recanalization-system-ref-bdrecansystem/) Recanalization systems may be in a manufacturing mode that allows the system to continuously run without the typical 30 second pauses, and 4-minute warning/5-minute restart required messages to indicate the ten-minute maximum catheter use time has been exce... Class II Reported ongoing Distribution: US: CA, OH, PA, NY, TX, NJ, MS, IL, GA, AL, AZ, NC, NV, PR, IN, MA, WI, KS, AR, FL, MD, IA, NE, LA, HI, MO, DE, DC, VA, NM, CO, KY, ME, MN [Official source for BD Recanalization System, REF: BDRECANSYSTEM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0676-2024%22) Nov 8, 2023 FDA device enforcement ### [Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM; 1610MSK/ Mission Kit 16G x 10CM; 1616MSK/ Missio...](https://isitonrecall.com/recall/fda-device-z-0643-2024-bard-mission-disposable-core-biopsy-instrument-kit-ref-name-1410msk-mission-kit-14g-x-10cm-1416msk-m/) The internal diameter of the coaxial cannula may be smaller or larger than the external diameter of the biopsy needle, and the length of the cannula may exceed the stated length on the label. As a result, the biopsy needle may not fit properly into the coax... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of PR, IL, MA, GA, KY, CA, TX, PA, IA, MN, NH, MD, FL, ID, IN, AL, VA, CO, WI, NY, NV, OK, OH, WA, MI, MS, AZ, HI,... [Official source for Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0643-2024%22) Aug 10, 2023 FDA device enforcement ### [Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016](https://isitonrecall.com/recall/fda-device-z-0027-2024-bard-marquee-disposable-core-biopsy-instrument-kit-ref-mqk2016/) Diameter mismatch between coaxial and biopsy needle (cutting cannula) in disposable core biopsy instrument kits, where the coaxial cannula inner diameter prohibits the biopsy needle (cutting cannula) from properly fitting into the coaxial cannula and access... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of PR, CO, TX, CA, WA, OR, AZ, NJ, NY, OH, NC, MD, MI, LA, IN, AK, TN and the countries of CA, AU, BE. [Official source for Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0027-2024%22) Apr 11, 2023 FDA device enforcement ### [Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM](https://isitonrecall.com/recall/fda-device-z-1564-2023-bard-mission-disposable-core-biopsy-instrument-kit-ref-2010msk-20g-x-10cm-ref-2016msk-20g-x-16cm/) Coaxial cannula internal diameter and length of biopsy instruments exceed the external diameter and length of the biopsy needle, prohibiting the biopsy needle from properly fitting into the coaxial cannula and accessing the target tissue, which could lead t... Class II Reported ongoing Distribution: US Nationwide Distribution: PR, 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, ND, NE, NH, NJ, NM, NV, NY, OH, O... [Official source for Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1564-2023%22) Feb 28, 2023 FDA device enforcement ### [Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK](https://isitonrecall.com/recall/fda-device-z-1260-2023-bard-mission-disposable-core-biopsy-instrument-kit-16g-x-10cm-ref-1610msk-18g-x-16cm-ref-1816msk/) The external diameter of the biopsy instrument is larger than the internal diameter of the coaxial needle, which could lead to: 1) Procedural delay, 2) Requirement of an additional device, 3), Needle tip breakage, if used despite incompatibility. Class II Reported ongoing Distribution: Worldwide Distribution: US (Nationwide) includes states of: FL, MD, OH, CO, PA, TX, NC, CA, ME, MO, NV, MI, IL, NY, VA, AZ, NH, LA, WI, KY, MA, WA, CT, SD, OK, DC, IA, AR, GA, N... [Official source for Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 18...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1260-2023%22) Jan 4, 2023 FDA device enforcement ### [Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter Repair Kit 0601620 6.6F Broviac CV Catheter Repair Kit 060163...](https://isitonrecall.com/recall/fda-device-z-1051-2023-catalog-number-product-description-0601600-2-7f-broviac-cv-catheter-repair-kit-0601610-4-2-fr-brovia/) Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable). Class II Reported ongoing Distribution: Worldwide Distribution: U.S.(nationwide): 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, ND, NE, NH, NJ, NM, NV,... [Official source for Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr B...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1051-2023%22) Dec 22, 2022 FDA device enforcement ### [The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a nitinol stent framework. The inner lumen of the covered stent is...](https://isitonrecall.com/recall/fda-device-z-1108-2023-the-covera-vascular-covered-stent-is-a-flexible-self-expanding-endoprothesis-comprised-of-eptfe-enca/) An increase in the reported complaint rate for inability to deploy was identified and related to poor slide block bonding. 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, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS,... [Official source for The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1108-2023%22) Apr 22, 2022 FDA device enforcement ### [REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,](https://isitonrecall.com/recall/fda-device-z-1273-2022-ref-pig1260k-6fr-x10-safe-t-centesis-catheter-drainage-kit-sterile-eo/) There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr needle instead of a 6 Fr needle. They can be used in conjunction with the following drainage methods: Universal extension set and drainage bag, vacuum bottle, and wall suction. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of MS, NC, FL, KS, GA, OH, AZ, NV, OH, IL, MI, MO,IA, CA, PA, AL,WA, TN, IN, NY and the countries of AU, BE, NZ. [Official source for REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1273-2022%22) Jan 20, 2022 FDA device enforcement ### [Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer](https://isitonrecall.com/recall/fda-device-z-0790-2022-safe-t-plus-pediatric-infant-lumbar-puncture-tray-22-g-x-1-5-spinal-needle-with-manometer/) Due to lumbar puncture tray manometer failure mode of leaking and mating issues. Class II Reported ongoing Distribution: U.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA,... [Official source for Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0790-2022%22) Jan 20, 2022 FDA device enforcement ### [LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5](https://isitonrecall.com/recall/fda-device-z-0791-2022-lumbar-puncture-tray-pediatric-21g-2-5/) Due to lumbar puncture tray manometer failure mode of leaking and mating issues. Class II Reported ongoing Distribution: U.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA,... [Official source for LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0791-2022%22) Jan 20, 2022 FDA device enforcement ### [LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP](https://isitonrecall.com/recall/fda-device-z-0792-2022-lumbar-puncture-tray-adult-20g-x-3-5-dp/) Due to lumbar puncture tray manometer failure mode of leaking and mating issues. Class II Reported ongoing Distribution: U.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA,... [Official source for LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0792-2022%22) Jan 20, 2022 FDA device enforcement ### [ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G](https://isitonrecall.com/recall/fda-device-z-0793-2022-adult-lumbar-puncture-drug-free-tray-20g/) Due to lumbar puncture tray manometer failure mode of leaking and mating issues. Class II Reported ongoing Distribution: U.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA,... [Official source for ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0793-2022%22) ## Reasons in these listed records - Due to damage to outer tray that can potentially compromise the sterile barrier - Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believe device is not yet ... - Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upo... - Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix ... These examples come from this result page and are not a ranking of every recall reason. ## Checking Bard Peripheral Vascular Inc ### Is there a recall on bard peripheral vascular inc right now? This archive contains 27 records, including 27 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 Peripheral Vascular Inc](https://isitonrecall.com/check/?q=Bard%20Peripheral%20Vascular%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)