Busse Hospital Disposables recalls Joint Injection Tray Catalog 856: Drug safety concerns due to uncertain test validation. Affected lot numbers: 2031105, 2130068, 2130167, 2130508, 2130862, 2131115.
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 Joint Injection Trays with specific catalog numbers due to drug safety concerns. The issue involves uncertain validation of test methods used to manufacture the drug products in these kits, which could affect safety.
The recall is due to uncertainty about whether the test methods used to manufacture the drug products were validated properly. This could mean the drugs might not be safe for use in medical procedures.
Healthcare professionals using these injection trays for medical procedures may be affected. Patients receiving treatments with these kits could be at risk if the drug products are unsafe.
Check for the catalog number 8561R1 on the Joint Injection Tray. Affected lots include 2031105, 2130068, 2130167, 2130508, 2130862, and 2131115.
Look for the catalog number 8561R1 and affected lot numbers on the Joint Injection Tray.
The recall is due to uncertainty about the adequacy of test methods used to manufacture the drug products, which could affect safety.
The official notice does not specify a remedy, so check with Busse Hospital Disposables for further instructions.
Affected lot numbers are 2031105, 2130068, 2130167, 2130508, 2130862, and 2131115.
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-1175-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1175-2022 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.
