Data Foundry

Medical device recalls 2026

A M S — Class I medical device recall Z-2622-2026

Ongoing recall by Windstone Medical Packaging, Inc., reported 2026-07-08, distributed nationwide. Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a

Recall numberZ-2622-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmWindstone Medical Packaging, Inc., Billings, MT, United States
Recall initiated2026-05-21
Classified2026-07-01
Reported by FDA2026-07-08
DistributedNationwide (US)
Quantity45 units
Lot numbers237663, 237901, 237957, 238041, 238084, 238085, 238146, 238197, 238589, 239157, 239216, 239286, 239337, 239386, 239943, 240269, 240633, 240705, 240903, 240904, 241034, 241223, 241224, 241313

Product

A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit

Reason for recall

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2622-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.