Abdominoplasty Pack recall: Sterility Concern
Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
Why was Abdominoplasty Pack recalled?
The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot numbers and Expiration dates: 80483, 1/19/2017 86796, 2/26/2018 88290, 2/7/2017 89931, 1/15/2018 98043, 9/7/2018 98446, 4/2/2019
- Product
- Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
- Recalling firm
- Windstone Medical Packaging, Inc.
- Quantity
- 45 kits
- Distribution
- Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
- Recall date
- March 8, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)