FDAClass IIDecember 21, 2022

Deroyal KIT Extremity Pack recall

DeRoyal KIT EXTREMITY PACK, REF 89-8869.09

Why was Deroyal KIT Extremity Pack recalled?

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What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

Lot Numbers: Lot 56390950 exp 6/1/2026; Lot 56837871 exp 9/1/2026; Lot 5718781 exp 10/1/2026

Product
DeRoyal KIT EXTREMITY PACK, REF 89-8869.09
Recalling firm
DeRoyal Industries Inc
Quantity
75 kits
Distribution
US: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi
Recall date
December 21, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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