Busse Hospital Disposables recalls SS 3.5MM Pellet Insert: Catalog B1354 with lot 2010304 due to uncertain drug test validation. Affected users should contact for details.
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
Busse Hospital Disposables is recalling their SS 3.5MM Pellet Insertion Tray with Medium Gloves (Catalog B1354) because drug safety tests may not have been properly validated. This could affect medical use if the product doesn't meet safety standards.
The recall is due to uncertainty about whether the drug test methods used to make the product were validated properly. This could mean the product might not be safe for medical use.
Healthcare professionals using the product for medical procedures are most at risk. Patients receiving treatments with this product may also be affected.
Check for Catalog Number B1354 and Lot Number 2010304 on the product. The product is sold under the brand Busse Hospital Disposables.
Reach out to Busse Hospital Disposables for specific guidance on the recall.
The recall is due to uncertainty about the validation of drug test methods used to manufacture the product.
Contact Busse Hospital Disposables for specific guidance on the recall.
The recall is for drug safety concerns, not direct injury risks. The official notice does not specify injury potential.
We’ve drafted a message you can send Busse Hospital Disposables to request your refund or repair — edit it as you like.
Subject: Recall Z-1183-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1183-2022 from Busse Hospital Disposables. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
