XP-XP Tibial Tray - Interlok 63 mm recall
XP-XP Tibial Tray - Interlok 63 mm Item # 195751
Why was XP-XP Tibial Tray - Interlok 63 mm recalled?
The locking bar not fully engaging
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 522520 571140 589700 758150 028960 028980 043970 028980R 043970R 064960 028970 065200 101860 101880 065200R 433940 321620 321640 321620R 321640R 433910 592120 592140 592150 592170 257970 592180 801960 282710 282710R 282690 801940 801950 783060 783040 011410 975550 592110 984660 023340 257960 840190 061310 592160 102990 223050 261130 336080 585400 585370 511430 467140 684820 664140 634080 705510 715730 716030 716030R 920550 881940 029210 906640 985880 072790 125870 162880 396240 318430 247250 336660 441870 374320 587220 509590 543180 543150 708390 576080 639600 670510 522580 558990 593560 450400 741460 758480 780160 808130 833150 873470 943480 850880 917590 183370 560280 570170 570180 570180R 076640 191080 111620 950910 963430 999270 018060 261910 613310 650370
- Product
- XP-XP Tibial Tray - Interlok 63 mm Item # 195751
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 480 units
- Distribution
- State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
- Recall date
- September 18, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)