CURAD REUSABLE GEL HOT/COLD PACK
Check against the official notice below — it lists the full affected range.
Medline Industries, LP is recalling CURAD Reusable Gel Hot/Cold Packs because the product contains natural rubber latex but the label does not indicate this. The affected packs were distributed in the US and several Caribbean and international locations, with approximately 494,273 units involved. The recalled products include Item Numbers CUR959/CUR959H and TGT0114V1, with specific lot numbers listed for each item number.
The source document does not specify a remedy or what affected consumers should do.
Written by software from the official notice below. Not reviewed by a lawyer.
The product contains natural rubber latex but the label states that it does not.
Reason for recall: The product contains natural rubber latex but the label states that it does not. Distribution: US and Bahamas, Bermuda, Panama, Lebanon, Barbados, Honduras, Anguilla Quantity: 494,273 ea Lot/code info: Item Numbers: 1) CUR959/CUR959H (Lots 69718070004, 69718090003, 69718100001, 69718100004, 69718110003, 69719010001, 69719030001, 69719030004, 69719040002, 69719070005, 69719080002, 69719080006, 69719090001, 69719090004, 69719100001, 69719100004, 69719110001, 69719110003, 69719110004, 69719120001, 69719120005, 69719120002, 69719120006, 69720010001, 69720020002, 69720040001, 69720050001, 69720060001, 69720060002, 69720080002, 69720090001, 69720090002, 69720100001, 69720100002, 69720110002, 69720120001, 69720120002, 69721010001, 69721020001, 69721030001, 69721030002, 69721050001, 69721050002, 69721050003, 69721060001, 69721060002, 69721070001, 69721080002, 69721090001) 2) TGT0114V1 (Lots 69718070004, 69718080002, 69718090002 , 69718100004, 69718110003, 69719010001, 69719030004, 69719040002, 69719050002, 69719050004, 69719060001, 69719060003, 69719070001, 69719070005, 69719080002, 69719080006, 69719090004, 69719100001, 69719100004, 69719100005, 69719110001, 69719110002, 69719110004, 69719110003, 69719120005, 69719120002, 69719120007, 69719120006, 69720010001, 69720070001, 69720070002, 69720080001, 69720080002, 69720100003)
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.