Windstone Custom Surgical Kits Recall: 3M Steri-Drape Drapes Contain Recalled Products
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.
Recall notice
Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes that have been recalled by 3M Healthcare.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/59783-windstone-custom-surgical-kits-recall-3m-steri-drape-drapes-contain.
Source Summary by GovInfoNow · govinfonow.com/recall/59783-windstone-custom-surgical-kits-recall-3m-steri-drape-drapes-contain · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0881-2023
Cite this page
“Windstone Custom Surgical Kits Recall: 3M Steri-Drape Drapes Contain Recalled Products.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59783-windstone-custom-surgical-kits-recall-3m-steri-drape-drapes-contain. Based on FDA recall #Z-0881-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0881-2023%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Windstone Medical Packaging- Category
Medical device
What to do — step by step
Check Product Details
Look for specific part numbers and lot numbers listed in the recall notice on the packaging of the surgical kits.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 14 states.
FDA distribution: “Worldwide distribution - U.S. Nationwide distribution in the states of AZ, CA, CO, CT, FL, Guam, IN, NC, NJ, NV, OK PA, TN, TX, and WI. The country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Colorado, Connecticut, Florida, Indiana, Nevada, New Jersey, North Carolina, Oklahoma, Pennsylvania, Tennessee, Texas, Wisconsin.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0881-2023 (November 1, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0881-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.