HipLOC Hip Fracture Fixation System-Hiploc System 135¿ recall
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression…
Why was HipLOC Hip Fracture Fixation System-Hiploc System 135¿ recalled?
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
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 Number: 3222067 3355792 3609499 3609508 3619245 3623355 3623356 3700289 3700610 3829536 3843022 3847671 3847672 3879198 3879199 3879200 3879202 3889526 3897103 3897106 3897115 3902248 3918363 3918364
- Product
- HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression…
- Recalling firm
- Biomet UK Ltd.
- Quantity
- 44 units
- Distribution
- US Nationwide in the states of AZ, MO, NJ and NM
- Recall date
- October 3, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)