FDAMay 30, 2023device

Custom medical procedure packs labeled as: a) OPEN HEART TRACECART, REF '53-1941; b) CARDIAC CATH PACK, REF '89-10045; c) SHOULDER PACK, REF '89-10115; d) MINOR ORTHO PACK, REF '89-10213; e) TOTAL KNEE PACK PGYBK, REF '89-10505; f) ANTERIOR HIP PACK PGYBK, REF '89-10563; g) ORTHO X-RAY PACK, REF ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.

What to do

FDA enforcement status: Ongoing

Brands named

deroyal

UPCs

507497568646760074975686467150749756980123007497569801285074975697790150749756350131007497563501365074975636312400749756363129507497563639880074975636398350749756214730

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Custom medical procedure packs labeled as: a) OPEN HEART TRACECART, REF '53-1941; b) CARDIAC CATH PACK, REF '89-10045; c) SHOULDER PACK, REF '89-10115; d) MINOR ORTHO PACK, REF '89-10213; e) TOTAL KNEE PACK PGYBK, REF '89-10505; f) ANTERIOR HIP PACK PGYBK, REF '89-10563; g) ORTHO X-RAY PACK, REF ... — Recall Details · AllClear