Reported Sep 14, 2022 · Ongoing
Medline CHEST TUBE REORDER NO: DYNJ36762A
Medline Industries 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: Medline Industries Inc. · 12001 General Milton · Laredo, TX · 78045
Is this the product you have?
- Medline CHEST TUBE REORDER NODYNJ36762A
- Lot codes and dates
- Model NumberDYNJ36762A UDI-DI Code (GTIN
- Insert/GTIN Case / Lot Number(01)1019348989440/(01)40193489894401 / 21ILA164 (01)1019348989440/(01)40193489894401 / 21ILA986 (01)1019348989440/(01)40193489894401 / 21JLA315 (01)1019348989440/(01)40193489894401 / 21KLA005 (01)1019348989440/(01)40193489894401 / 21KLA162 (01)1019348989440/(01)40193489894401 / 21KLA629
- Amount recalled
- 300 kits
Where it was sold
- Nationwide
- AL
Why it was recalled
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
This product could cause temporary or reversible health problems — stop using it.
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