FDA Device recall Z-1862-2017

various polyethylene implants Custom parts Product Usage: Custom

FDA Device
Class II
terminated
Published 2017-04-26

On 2017-04-26 the FDA classified a Class II recall of various polyethylene implants Custom parts Product Usage: Custom by Zimmer Biomet, citing endotoxin levels higher than process maximum limits were discovered in the identified polyethylene components.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1862-2017
Classification	Class II
Status	terminated
Initiated	2017-02-17
Published	2017-04-26
Last updated	2026-09-13 11:54 UTC
Company	Zimmer Biomet
Distribution	US

Product

various polyethylene implants Custom parts Product Usage: Custom

Reason

Endotoxin levels higher than process maximum limits were discovered in the identified polyethylene components.

Identifiers

code_info	Items and lots: Item 110010452 732130 920720 Item 110010454 136510 Item 110010455 752320 896040 Item 110010456… Items and lots: Item 110010452 732130 920720 Item 110010454 136510 Item 110010455 752320 896040 Item 110010456 383320 879930 Item 110010459 854290 879950 905350 Item 110010462 752460 778490 Item 110010468 827730 Item 110010476 827530 827540 Item 110010716 753050 ItemCP753453 655990 ItemCP753455 656110 ItemCP753461 382210 Item CP753470 436530 Item CP753476 502920 Item CP753478 524950 Item CP753480 436460 Item CP753486 655300 Item CP753488 655470 Item CP753494 467390 Item CP753496 467420 Item CP753502 448730 Item CP753504 453990 Item CP753506 454640 Item CP753508 502970 Item CP753510 831310 Item CP753512 654720 Item CP753514 594570 Item CP753517 594630 Item CP753519 534820 Item CP753521 535090 Item CP753523 654190 Item CP753525 674160 Item CP753531 691490 Item CP753533 691560 Item CP753535 691640 Item CP753537 691680 Item CP753547 691720 Item CP753549 696620

code_info

Items and lots: Item 110010452 732130 920720 Item 110010454 136510 Item 110010455 752320 896040 Item 110010456…

Items and lots: Item 110010452 732130 920720 Item 110010454 136510 Item 110010455 752320 896040 Item 110010456 383320 879930 Item 110010459 854290 879950 905350 Item 110010462 752460 778490 Item 110010468 827730 Item 110010476 827530 827540 Item 110010716 753050 ItemCP753453 655990 ItemCP753455 656110 ItemCP753461 382210 Item CP753470 436530 Item CP753476 502920 Item CP753478 524950 Item CP753480 436460 Item CP753486 655300 Item CP753488 655470 Item CP753494 467390 Item CP753496 467420 Item CP753502 448730 Item CP753504 453990 Item CP753506 454640 Item CP753508 502970 Item CP753510 831310 Item CP753512 654720 Item CP753514 594570 Item CP753517 594630 Item CP753519 534820 Item CP753521 535090 Item CP753523 654190 Item CP753525 674160 Item CP753531 691490 Item CP753533 691560 Item CP753535 691640 Item CP753537 691680 Item CP753547 691720 Item CP753549 696620

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1862-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.