Windstone Medical Packaging recalls Aligned Medical Tonsil Packs with Cardinal Health Salem Sump PVC tubes (AMS14809) due to improper use risks. Affected units include specific lot numbers.
Due to convenience kits containing a kit component that is under a recall action for improper use.
Windstone Medical Packaging recalls Aligned Medical Tonsil Packs (REF AMS14809) that contain Cardinal Health Salem Sump PVC tubes. The recall is due to a convenience kit component being under a separate recall for improper use.
The hazard involves a convenience kit component that has been recalled for improper use. This could lead to unsafe handling during clinical procedures if not addressed.
Healthcare providers using the Aligned Medical Tonsil Packs for clinical procedures are likely affected. Those with specific lot numbers (192737, 194922, 200224, 200950, 203412) are at risk.
Check for the product name 'Aligned Medical Tonsil Pack' with reference number AMS14809. Look for lot numbers: 192737, 194922, 200224, 200950, or 203412.
Identify the lot number on the packaging to confirm if it matches the affected numbers: 192737, 194922, 200224, 200950, or 203412.
The convenience kit component in this product is under a separate recall for improper use.
Lot numbers 192737, 194922, 200224, 200950, and 203412.
The recall does not specify a stop-use action; check the lot number to determine if it is affected.
We’ve drafted a message you can send Windstone Medical Packaging to request your refund or repair — edit it as you like.
Subject: Recall Z-0031-2025 — Windstone Medical Packaging Windstone Medical Packaging Hello, I own a Windstone Medical Packaging that is covered by recall Z-0031-2025 from Windstone Medical Packaging. 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.