Hoffman LRF Hexapod Strut recall
Hoffman LRF Hexapod Strut, Extra Short 105mm-139mm, Model Number 4935-0-020. Product Usage - The Hoffmann LRF System is indicated in pediatric…
Why was Hoffman LRF Hexapod Strut recalled?
The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in partial of full displacement or loss of the pin and, accordingly, stability of the strut of the frame cannot be ensured.
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?
Lots: L18237 L13688 L22248 L25187 L31271 L35846 L46782 L47078 L47196 L50180 L51361 L53108 L53489 L57504 L58108 L57506 Y00082 Y02871 Y03127 Y08559 Y08560 Y12875 Y14371 Y14640 Y14644 Y14645
- Product
- Hoffman LRF Hexapod Strut, Extra Short 105mm-139mm, Model Number 4935-0-020. Product Usage - The Hoffmann LRF System is indicated in pediatric…
- Recalling firm
- Stryker GmbH
- Quantity
- 832
- Distribution
- US Nationwide in the states of CO, FL, MD, MI, NY, OK, and PA.
- Recall date
- November 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)