Shoulder Pack, Kit number AMS1372(A, AMS1372(B, AMS2335, AMS2335(A, AMS2936, AMS3638, AMS3711, AMS4212, PSS1852(A, convenience custom kits used for general surgery in hospital operating room
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Number/ Expiration Date: 61069 1/5/2015 57470 1/15/2015 64162 1/20/2015 66792 1/31/2015 61312 2/27/2015 66392 2/27/2015 59327 4/24/2015 60099 7/15/2015 61872 7/26/2015 60277 8/24/2015 60278 8/24/2015 61393 9/7/2015 63201 9/15/2015 61394 10/14/2015 62762 11/3/2015 61940 11/17/2015 62155 11/23/2015 64557 11/27/2015 61280 11/27/2015 61279 11/28/2015 61392 11/30/2015 66184 12/24/2015 65278 12/27/2015 63178 1/3/2016 63994 1/13/2016 64601 1/13/2016 64643 1/17/2016 63782 1/23/2016 63783 1/23/2016 73045 1/29/2016 69613 2/19/2016 69677 4/9/2016 70513 4/11/2016 76391 4/13/2016 74109 4/24/2016 57074 5/25/2016 76644 5/30/2016 57513 6/20/2016 71983 7/15/2016 67297 7/20/2016 67764 7/20/2016 58232 7/24/2016 58465 7/25/2016 77327 7/26/2016 77744 7/30/2016 78161 7/30/2016 65887 8/1/2016 67940 8/23/2016 68760 9/22/2016 70301 9/22/2016 70693 10/7/2016 69712 10/26/2016 68631 10/31/2016 71525 12/18/2016 71460 1/3/2017 72471 1/10/2017 72320 1/15/2017 70770 1/21/2017 72628 1/21/2017 73287 1/23/2017 72147 1/24/2017 72387 1/26/2017 72082 1/26/2017 72859 3/9/2017 72963 3/28/2017 73114 3/28/2017 76279 4/24/2017 76886 4/24/2017 74673 5/22/2017 75245 6/21/2017 76449 7/14/2017 77055 7/19/2017 77333 8/11/2017 78762 9/19/2017 78747 9/20/2017 79341 11/19/2017 79919 1/23/2018 73790 (no date was provided)
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Windstone Medical Packaging, Inc.
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Shoulder Pack, Kit number AMS1372(A, AMS1372(B, AMS2335, AMS2335(A, AMS2936, AMS3638, AMS3711, AMS4212, PSS1852(A, convenience custom kits used for general surgery in hospital operating room
Product Codes/Lot Numbers:
Lot Number/ Expiration Date: 61069 1/5/2015 57470 1/15/2015 64162 1/20/2015 66792 1/31/2015 61312 2/27/2015 66392 2/27/2015 59327 4/24/2015 60099 7/15/2015 61872 7/26/2015 60277 8/24/2015 60278 8/24/2015 61393 9/7/2015 63201 9/15/2015 61394 10/14/2015 62762 11/3/2015 61940 11/17/2015 62155 11/23/2015 64557 11/27/2015 61280 11/27/2015 61279 11/28/2015 61392 11/30/2015 66184 12/24/2015 65278 12/27/2015 63178 1/3/2016 63994 1/13/2016 64601 1/13/2016 64643 1/17/2016 63782 1/23/2016 63783 1/23/2016 73045 1/29/2016 69613 2/19/2016 69677 4/9/2016 70513 4/11/2016 76391 4/13/2016 74109 4/24/2016 57074 5/25/2016 76644 5/30/2016 57513 6/20/2016 71983 7/15/2016 67297 7/20/2016 67764 7/20/2016 58232 7/24/2016 58465 7/25/2016 77327 7/26/2016 77744 7/30/2016 78161 7/30/2016 65887 8/1/2016 67940 8/23/2016 68760 9/22/2016 70301 9/22/2016 70693 10/7/2016 69712 10/26/2016 68631 10/31/2016 71525 12/18/2016 71460 1/3/2017 72471 1/10/2017 72320 1/15/2017 70770 1/21/2017 72628 1/21/2017 73287 1/23/2017 72147 1/24/2017 72387 1/26/2017 72082 1/26/2017 72859 3/9/2017 72963 3/28/2017 73114 3/28/2017 76279 4/24/2017 76886 4/24/2017 74673 5/22/2017 75245 6/21/2017 76449 7/14/2017 77055 7/19/2017 77333 8/11/2017 78762 9/19/2017 78747 9/20/2017 79341 11/19/2017 79919 1/23/2018 73790 (no date was provided)
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0270-2017
Related Recalls
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
Windstone Medical Packaging
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 connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
Windstone Medical Packaging
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 utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994A
Windstone Medical Packaging
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 utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).