Morris Hysto Pack recall: Sterility Concern
Morris Hysto Pack, part number PSS3198(A
Why was Morris Hysto 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 101121, 10/5/2019 101680, 10/27/2019 83882, 7/8/2018 87088, 8/16/2018 87496, 9/24/2018 88351, 11/11/2018 89549, 12/22/2018 94996, 1/30/2019 97899, 6/15/2019 98769, 6/25/2019
- Product
- Morris Hysto Pack, part number PSS3198(A
- Recalling firm
- Windstone Medical Packaging, Inc.
- Quantity
- 156 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)