Affixus¿ Hip Fracture Nail 125¿ 11 mm x 180 mm recall
Affixus¿ Hip Fracture Nail 125¿ 11 mm x 180 mm, Item Number: 814311180
Why was Affixus¿ Hip Fracture Nail 125¿ 11 mm x 180 mm recalled?
The set screw is not able to advance or reverse from the original position in the nail.
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?
017190 017200 017210 017240 017260 063270 063330 063360 063370 063400 087850 087870 097080 132740 153330 153470 153490 153510 153540 219770 219780 290570 290580 290620 500680 500710 500740 503300 503350 519650 565790 565800 585690 601380 628190 645550 645580 688170 688190 688200 688210 707670 741680 741690 741700 899820 899840 899850 899870 899880 900000
- Product
- Affixus¿ Hip Fracture Nail 125¿ 11 mm x 180 mm, Item Number: 814311180
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 5947 total
- Distribution
- The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WY, and Puerto Rico. The products were distributed to the following foreign countries: Chile, Ecuador, Japan, Netherlands.
- Recall date
- September 19, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)