FDAJanuary 11, 2016device

Product 56 consists of all product under product code: HWC and same usage: Item no: 47234702032 PERI SCR 3.5MM X 32MM STE 47234702018 PERI SCR. 3.5MM X 18MM ST 47234702020 PERI SCR. 3.5MM X 20MM ST 47234702022 PERI SCR. 3.5MM X 22MM ST 47234702026 PERI SCR. 3.5MM X 26MM ST 47234702030 PERI SCR. 3...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

zimmer manufacturing b vzimmerzimmer manufacturing

UPCs

472347020324723470201847234702020472347020224723470202647234702030472347020344723470203647234702042472347020464723470205047234702080

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Product 56 consists of all product under product code: HWC and same usage: Item no: 47234702032 PERI SCR 3.5MM X 32MM STE 47234702018 PERI SCR. 3.5MM X 18MM ST 47234702020 PERI SCR. 3.5MM X 20MM ST 47234702022 PERI SCR. 3.5MM X 22MM ST 47234702026 PERI SCR. 3.5MM X 26MM ST 47234702030 PERI SCR. 3... — Recall Details · AllClear