Busse Hospital Disposables recalls SS 3.5Mm Pel: 2110100-2110262 lot numbers due to uncertain drug product validation methods. Affected users should check their catalog number and lot numbers.
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 SS 3.5Mm Pellet Insertion Trays with catalog number B1352R1 because drug products in these kits may have uncertain validation methods. This could affect the safety of the drug products used in medical procedures.
The recall is due to uncertainty about whether the drug products in these kits were properly validated during manufacturing. This uncertainty could lead to potential safety issues with the drug products.
Healthcare professionals using these trays for medical procedures are most at risk. Patients receiving treatments with these products may be affected.
Check for catalog number B1352R1 and lot numbers 2110100, 2110083, 2110226, or 2110262 on the product packaging.
Identify the catalog number and lot numbers on the product packaging to confirm if it is affected.
The recall is due to uncertainty about the adequacy of validation methods used to manufacture the drug products in these kits.
The official recall notice does not specify a remedy or action steps for affected products.
Look for catalog number B1352R1 and lot numbers 2110100, 2110083, 2110226, or 2110262 on the product packaging.
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-1182-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1182-2022 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.
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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.
