RecallRadar

FDA Device recall Z-0472-2013

OSS Reamer Sleeve REF132-472662 KNEE REAMER SLEEVE 13.0 thru 20.0 STAINLESS STEEL The OSS Knee Reamer Sleeves are primarily used to guide t…

On 2012-12-12 the FDA classified a Class II recall of OSS Reamer Sleeve REF132-472662 KNEE REAMER SLEEVE 13.0 thru 20.0 STAINLESS STEEL The OSS Knee Reamer Sleeves are primarily used to guide t… by Biomet, citing biomet has initiated this action following an investigation which identified that the thin shaft reamer may get stuck and not slide into the sleeve.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0472-2013
ClassificationClass II
Statusterminated
Initiated2012-11-01
Published2012-12-12
Last updated2026-09-13 11:53 UTC
CompanyBiomet
DistributionUS

Product

OSS Reamer Sleeve REF132-472662 KNEE REAMER SLEEVE 13.0 thru 20.0 STAINLESS STEEL The OSS Knee Reamer Sleeves are primarily used to guide the bullet tip of cylindrical reamers during the tibial preparation in OSS procedures. They are reusable.

Reason

Biomet has initiated this action following an investigation which identified that the thin shaft reamer may get stuck and not slide into the sleeve.

Identifiers

code_infoPart Numbers 32-472662, 13.0 thru 20.0 Lot 154590, 156980, 519470, 519480, 542290, 628890, 755530

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0472-2013%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.