Hinge Coupling Hoffmann LRF recall
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity…
Why was Hinge Coupling Hoffmann LRF recalled?
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
What should I do if I have this product?
Review the official FDA enforcement record for current 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 # L23745
- Product
- Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity…
- Recalling firm
- Stryker GmbH
- Quantity
- 18
- Distribution
- USA (nationwide) Distribution
- Recall date
- May 2, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)