Lap/Pelviscopy Pack recall: Sterility Concern
Lap/Pelviscopy Pack, part number PSS3256(B
Why was Lap/Pelviscopy 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 number and expiration date 85327, 7/14/2018 88019, 9/5/2018 88577, 12/27/2018 89638, 1/29/2019 95231, 1/12/2019 95423, 1/2/2019 96080, 6/21/2019 99559, 6/5/2019
- Product
- Lap/Pelviscopy Pack, part number PSS3256(B
- Recalling firm
- Windstone Medical Packaging, Inc.
- Quantity
- 168 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)