Deroyal Posterior Lumbar Fusion Pack recall
DeRoyal POSTERIOR LUMBAR FUSION PACK, REF 89-10060.02
Why was Deroyal Posterior Lumbar Fusion 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 56395179 exp 12/1/2023; Lot 56431133 exp 9/1/2023; Lot 57190554 exp 3/1/2024; Lot 5740754 exp 4/1/2024
- Product
- DeRoyal POSTERIOR LUMBAR FUSION PACK, REF 89-10060.02
- Recalling firm
- DeRoyal Industries Inc
- Quantity
- N/A
- 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)