Windstone Medical Packaging recalls custom surgical instrument disposable kits containing 3M Steri-Drape surgical drapes that were previously recalled by 3M Healthcare. Affected kits include various surgical packs with specific part numbers and lot numbers.
Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes that have been recalled by 3M Healthcare.
Windstone Medical Packaging is recalling various custom surgical instrument disposable kits that contain 3M Steri-Drape surgical drapes. These kits were previously recalled by 3M Healthcare due to potential safety issues with the drapes.
The recall is triggered by 3M Healthcare's prior recall of 3M Steri-Drape surgical drapes. However, the specific hazard mechanism is not clearly described in this record, so the risk level cannot be determined.
Medical professionals and hospitals that use these surgical kits are likely affected. Patients undergoing surgery with these kits may be at risk if the drapes are not properly handled.
Check for kits with part numbers listed in the record, such as AMS10411A Nasal Endoscopy Pack or VPP1020A Custom Dental Pack. Look for lot numbers like 172743, 175939, or 178701 on the packaging.
Look for specific part numbers and lot numbers listed in the recall notice on the packaging of the surgical kits.
The recall is due to 3M Healthcare's prior recall of 3M Steri-Drape surgical drapes. The specific hazard mechanism is not clearly described in this record.
Check for kits with part numbers like AMS10411A or VPP1020A and lot numbers such as 172743, 175939, or 178701 on the packaging.
The recall record does not specify a remedy, so contact Windstone Medical Packaging directly for guidance.
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-0881-2023 — Windstone Medical Packaging Windstone Medical Packaging Hello, I own a Windstone Medical Packaging that is covered by recall Z-0881-2023 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.
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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.
