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Windstone Medical Packaging Recalls
336 recalls on record · December 16, 2015 to August 5, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 26, 2016Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Abdominoplasty Pack, Kit number AMS3326 convenience custom kits used for general surgery in hospital operating room
Hazard: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.
June 8, 2016Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls General Surgery Pack, part number 006880-3. This is a custom convenience surgical instrument disposable kit. There
Hazard: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges which were recalled by Medtronic due to the potential for sterile barrier to be comprised at the packaging seal.
June 8, 2016Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Laparotomy Pack Latex Free, part number 007725-7. This is a custom convenience surgical instrument disposable kit.
Hazard: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges which were recalled by Medtronic due to the potential for sterile barrier to be comprised at the packaging seal.
June 8, 2016Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Laparotomy Pack, Part numbers 006268-8 and 007725-8. This is a custom convenience surgical instrument disposable kit.
Hazard: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges which were recalled by Medtronic due to the potential for sterile barrier to be comprised at the packaging seal.
December 16, 2015Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls AMS 4675 Angio Pack. For use in a general clinical procedure.
Hazard: AMS 4675 Angio Pack is recalled because this kit containing U-SDN 2 Part Ultra Modified Seldinger Needle which is recalled by supplier.
December 16, 2015Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls AMS 4674 Custom Pack. For use in a general clinical procedure.
Hazard: AMS 4674 Custom Pack is recalled because this kit containing U-SDN 2 Part Ultra Modified Seldinger Needle which is recalled by supplier.