Busse Hospital Disposables recalls Epidural Tray Catalog 1577 (lot numbers 2130426, 2:130801, etc.) due to uncertainty in drug manufacturing validation. Affected users should contact the manufacturer 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 Epidural Tray Catalog 1577 because drug products in the kit may not have been properly validated during manufacturing. This could affect medical use and requires contacting the manufacturer for specific details.
The drug products in the kit were manufactured using test methods that may not have been adequately validated. This uncertainty could lead to potential issues with the drug's safety and effectiveness during medical use.
Healthcare professionals using the Epidural Tray Catalog 1577 in medical procedures are most at risk. Patients receiving these products may also be affected.
Check for lot numbers 2130426, 2130801, 2131032, 2131138, or 2131290 on the Epidural Tray Catalog 1577. The UDI code 00849233006546 is also associated with this recall.
Reach out to Busse Hospital Disposables for specific instructions on handling the recalled product.
The recall is for Epidural Tray Catalog 1577 with specific lot numbers and UDI code.
Check for lot numbers 2130426, 2130801, 2131032, 2131138, or 2131290 on the product.
Contact Busse Hospital Disposables for specific instructions on handling the recalled product.
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-1155-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1155-2022 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.
