RecallRadar

FDA Device recall Z-1159-2016

Product 61 consists of all product under product code: JWH and same usage: Item no: 598003712 STD PRECOAT TIBIA PLATE S for use in total kn…

On 2016-03-23 the FDA classified a Class II recall of Product 61 consists of all product under product code: JWH and same usage: Item no: 598003712 STD PRECOAT TIBIA PLATE S for use in total kn… by Zimmer Manufacturing B V, citing as a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1159-2016
ClassificationClass II
Statusterminated
Initiated2016-01-11
Published2016-03-23
Last updated2026-09-13 11:54 UTC
CompanyZimmer Manufacturing B V
DistributionUS

Product

Product 61 consists of all product under product code: JWH and same usage: Item no: 598003712 STD PRECOAT TIBIA PLATE S for use in total knee arthroplasty

Reason

As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.

Identifiers

code_info
lot no.: 61678240 61838251 61838252 61838253 61838254 61901158 61901159 61925016 61926797 61958844 61958845…lot no.: 61678240 61838251 61838252 61838253 61838254 61901158 61901159 61925016 61926797 61958844 61958845 61999206 61999207 62037903 62037904 62037905 62070148 62070149 62141260 62170961 62191179 62220224 62232384 62245104 62284609 62298550 62298551 62313021 62319305 62326309 62359946

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-1159-2016%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.