Windstone Medical Packaging recalls
9 recent recalls on record for Windstone Medical Packaging in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.
Models with recalls
All Windstone Medical Packaging recalls
FDA Class I · Medical device · July 8, 2026
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 …
Official ID Z-2622-2026 ·
Official record ↗
FDA Class I · Medical device · July 8, 2026
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 …
Official ID Z-2621-2026 ·
Official record ↗
FDA Class I · Medical device · July 8, 2026
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 …
Official ID Z-2620-2026 ·
Official record ↗
FDA Class I · Medical device · July 8, 2026
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 …
Official ID Z-2619-2026 ·
Official record ↗
FDA Class II · Medical device · June 10, 2026
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
Official ID Z-2307-2026 ·
Official record ↗
FDA Class I · Medical device · May 20, 2026
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose …
Official ID Z-2066-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …
Official ID Z-1921-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …
Official ID Z-1920-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …
Official ID Z-1919-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.