--- title: "Busse Hospital Disposables, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Busse Hospital Disposables, 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/busse-hospital-disposables-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Busse Hospital Disposables, Inc. recall records **5** reported ongoing 63 records in this archive. Latest source date Nov 30, 2023. 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 Nov 30, 2023 FDA device enforcement ### [Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE](https://isitonrecall.com/recall/fda-device-z-0592-2024-catalog-no-800-tracheostomy-care-tray-sterile-latex-free/) Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance level (SAL) of 10^-6 cannot be guaranteed. Risks to patients if produc... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0592-2024%22) Nov 30, 2023 FDA device enforcement ### [Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE](https://isitonrecall.com/recall/fda-device-z-0593-2024-catalog-no-1443-dressing-change-tray-sterile-latex-free/) Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance level (SAL) of 10^-6 cannot be guaranteed. Risks to patients if produc... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0593-2024%22) Nov 30, 2023 FDA device enforcement ### [Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / STERILE - LATEX FREE](https://isitonrecall.com/recall/fda-device-z-0594-2024-catalog-no-9251r1-9251r2-9251r3-tracheostomy-care-set-sterile-latex-free/) Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance level (SAL) of 10^-6 cannot be guaranteed. Risks to patients if produc... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / STERILE - LATEX FREE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0594-2024%22) Oct 21, 2022 FDA device enforcement ### [Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1](https://isitonrecall.com/recall/fda-device-z-0325-2023-busse-joint-injection-tray-intended-as-a-nerve-block-ref-no-8561-r1/) Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable Class II Reported ongoing Distribution: TX [Official source for Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0325-2023%22) Oct 21, 2022 FDA device enforcement ### [Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1](https://isitonrecall.com/recall/fda-device-z-0326-2023-busse-spine-injection-tray-intended-as-a-nerve-block-ref-no-8563r1/) Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable Class II Reported ongoing Distribution: TX [Official source for Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0326-2023%22) Feb 22, 2022 FDA device enforcement ### [I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Prevantics Catalog Number: 822](https://isitonrecall.com/recall/fda-device-z-1147-2022-i-v-start-kit-tegaderm-dressing-catheter-securement-prevantics-catalog-number-822/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Prevantics Catalog Number: 822](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1147-2022%22) Feb 22, 2022 FDA device enforcement ### [Procedure Tray Catalog 1065](https://isitonrecall.com/recall/fda-device-z-1148-2022-procedure-tray-catalog-1065/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Procedure Tray Catalog 1065](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1148-2022%22) Feb 22, 2022 FDA device enforcement ### [Cervical Tray Catalog 1089](https://isitonrecall.com/recall/fda-device-z-1149-2022-cervical-tray-catalog-1089/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Cervical Tray Catalog 1089](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1149-2022%22) Feb 22, 2022 FDA device enforcement ### [Lumbar Tray Catalog 1091](https://isitonrecall.com/recall/fda-device-z-1150-2022-lumbar-tray-catalog-1091/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Lumbar Tray Catalog 1091](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1150-2022%22) Feb 22, 2022 FDA device enforcement ### [Single Shot Epidural Tray Catalog 1165](https://isitonrecall.com/recall/fda-device-z-1151-2022-single-shot-epidural-tray-catalog-1165/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Single Shot Epidural Tray Catalog 1165](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1151-2022%22) Feb 22, 2022 FDA device enforcement ### [Single Shot Epidural Tray Catalog 1292](https://isitonrecall.com/recall/fda-device-z-1152-2022-single-shot-epidural-tray-catalog-1292/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Single Shot Epidural Tray Catalog 1292](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1152-2022%22) Feb 22, 2022 FDA device enforcement ### [Epidural Tray Catalog 1307](https://isitonrecall.com/recall/fda-device-z-1153-2022-epidural-tray-catalog-1307/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Epidural Tray Catalog 1307](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1153-2022%22) Feb 22, 2022 FDA device enforcement ### [Universal Tray Catalog 1567](https://isitonrecall.com/recall/fda-device-z-1154-2022-universal-tray-catalog-1567/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Universal Tray Catalog 1567](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1154-2022%22) Feb 22, 2022 FDA device enforcement ### [Epidural Tray Catalog 1577](https://isitonrecall.com/recall/fda-device-z-1155-2022-epidural-tray-catalog-1577/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Epidural Tray Catalog 1577](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1155-2022%22) Feb 22, 2022 FDA device enforcement ### [Port Tray Catalog 7607](https://isitonrecall.com/recall/fda-device-z-1156-2022-port-tray-catalog-7607/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Port Tray Catalog 7607](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1156-2022%22) Feb 22, 2022 FDA device enforcement ### [I.V. Start Kit Catalog 8172](https://isitonrecall.com/recall/fda-device-z-1157-2022-i-v-start-kit-catalog-8172/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for I.V. Start Kit Catalog 8172](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1157-2022%22) Feb 22, 2022 FDA device enforcement ### [Nerve Block Tray Catalog Number: 8415](https://isitonrecall.com/recall/fda-device-z-1158-2022-nerve-block-tray-catalog-number-8415/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Nerve Block Tray Catalog Number: 8415](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1158-2022%22) Feb 22, 2022 FDA device enforcement ### [Single Shot Epidural Tray Catalog Number: 8417](https://isitonrecall.com/recall/fda-device-z-1159-2022-single-shot-epidural-tray-catalog-number-8417/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Single Shot Epidural Tray Catalog Number: 8417](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1159-2022%22) Feb 22, 2022 FDA device enforcement ### [Nerve Block Tray Catalog Number: 9342](https://isitonrecall.com/recall/fda-device-z-1160-2022-nerve-block-tray-catalog-number-9342/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Nerve Block Tray Catalog Number: 9342](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1160-2022%22) Feb 22, 2022 FDA device enforcement ### [Universal Nerve Block Tray Catalog Number: 9779](https://isitonrecall.com/recall/fda-device-z-1161-2022-universal-nerve-block-tray-catalog-number-9779/) Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufac... Class II Reported terminated Distribution: Nationwide [Official source for Universal Nerve Block Tray Catalog Number: 9779](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1161-2022%22) ## Reasons in these listed records - Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance level (SAL) of 10^-6 cannot be guaranteed. Risks to patients if product is used include bl... - Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable - Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products These examples come from this result page and are not a ranking of every recall reason. ## Checking Busse Hospital Disposables, Inc. ### Is there a recall on busse hospital disposables, inc. right now? This archive contains 63 records, including 5 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 Busse Hospital Disposables, Inc.](https://isitonrecall.com/check/?q=Busse%20Hospital%20Disposables%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)