RecallRadar

FDA Device recall Z-0093-2027

GYN LAPAROSCOPY/LAPAROTOMY

On 2026-10-14 the FDA classified a Class II recall of GYN LAPAROSCOPY/LAPAROTOMY by Avid Medical, citing product may be potentially contaminated with a lubricant used during the manufacturing process.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0093-2027
ClassificationClass II
Statusongoing
Initiated2026-08-10
Published2026-10-14
Last updated2026-10-21 05:30 UTC
CompanyAvid Medical
DistributionUS

Product

GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;

Reason

Product may be potentially contaminated with a lubricant used during the manufacturing process.

Identifiers

code_info
1. Model/Item Number (Kit): WRNM002-15; UDI-DI: 10809160487181; Kit Lot Numbers: 1666722; 2. Model/Item Number (Kit):…1. Model/Item Number (Kit): WRNM002-15; UDI-DI: 10809160487181; Kit Lot Numbers: 1666722; 2. Model/Item Number (Kit): FBCH108-03; UDI-DI: 10809160399781; Kit Lot Numbers: 1659079, 1696378; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKU3975, NGKU2887;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-21 05:30 UTC. Current status: ongoing.

Other recalls by Avid Medical

All Avid Medical recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0093-2027%22

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