Hoffman LRF Hexapod Strut recall
Hoffman LRF Hexapod Strut, Extra Short 131mm-191mm, Model Number 4935-0-030. 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: L18238 L13689 L22249 L26333 L31075 L31035 L35849 L35850 L45970 L46580 L47080 L46577 L46781 L47195 L49918 L49816 L51362 L53106 L53487 L53823 L53488 L56830 L56831 L57502 Y00081 Y00080 Y02872 Y02873 Y03128 Y07628 Y07630 Y08561 Y08555 Y08554 Y08553 Y12876 Y14867 Y14641
- Product
- Hoffman LRF Hexapod Strut, Extra Short 131mm-191mm, Model Number 4935-0-030. Product Usage - The Hoffmann LRF System is indicated in pediatric…
- Recalling firm
- Stryker GmbH
- Quantity
- 1355
- 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)