Reported Oct 30, 2019 · Terminated
Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap
Andover Healthcare Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Andover Healthcare Inc. · 9 Fanaras Dr · Salisbury, MA · 01952-1444
Is this the product you have?
- Sterile Co-Flex Med 3" -
- Product UsageSingle Use secondary wound dressing or compression wrap
- Lot codes and dates
- Manufacturer's product or Catalog # 7300S
- Expiration Date01OCT2021-14JUN2022
- LotCI10LN
- Amount recalled
- 269 Cases
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Incomplete packaging seal of sterile product
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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