Sterile Co-Flex Med 3" - Product Usage: Single Use recall
Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap
Why was Sterile Co-Flex Med 3" - Product Usage: Single Use recalled?
Incomplete packaging seal of sterile product
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?
Manufacturer's product or Catalog # 7300S Expiration Date: 01OCT2021-14JUN2022 Lot : CI10LN
- Product
- Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap
- Recalling firm
- Andover Healthcare Inc.
- Quantity
- 269 Cases
- Distribution
- US Nationwide distribution including the states of MA, TX, RI, OH, NY, MN, SD, IL, MO, FL, VA, NE, UT, CA
- Recall date
- October 30, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)