RecallRadar

FDA Device recall Z-1819-2016

Various trauma and sports medicine instruments and implants

On 2016-06-01 the FDA classified a Class II recall of Various trauma and sports medicine instruments and implants by Biomet, citing insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If th….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1819-2016
ClassificationClass II
Statusterminated
Initiated2016-04-01
Published2016-06-01
Last updated2026-09-13 11:54 UTC
CompanyBiomet
DistributionUS

Product

Various trauma and sports medicine instruments and implants. Rod, fixation, intramedullary and accessories.

Reason

Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.

Identifiers

code_info
Part #'s 28234 28338 28811 28813 28821 29260 29822 805065080 14-400428 14-400436 14-405032 14-405040 14-44…Part #'s 28234 28338 28811 28813 28821 29260 29822 805065080 14-400428 14-400436 14-405032 14-405040 14-440118 14-440121 14-441280 14-440066S Lot #'s 590970 591080 591090 665210 692040 692250 692280 692290 695900 610470 665230 665240 692440 692450 692480 692620 692660 692670 692690 721680 721720 721730 729080 722730 621840 621860 678300 664740 664820 664870 664880 503760 503770 693840 476230

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-1819-2016%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.