AVID Medical Recalls Urology Kits for Potential Lubricant Contamination
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as Class II due to potential contamination with a manufacturing lubricant. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
AVID Medical, Inc. is recalling 20 Urology Major kits, Model/Item Number WRNM058-10. The recall is due to the potential for contamination with a lubricant used during the manufacturing process. The affected kits have UDI-DI 10809160488898 and Kit Lot Number 1681989. The recalled supplier component within the kits is A902416 with Lot Number NGKU2887.
The affected products were distributed nationwide in the states of Arizona, California, Florida, Maryland, Nebraska, and Texas. The source text does not report any illnesses, injuries, or deaths associated with this recall.
Consumers and healthcare providers should stop using the affected kits and contact AVID Medical, Inc. for further instructions or a return.
The recalled product
- Product
- UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
- Manufacturer
- AVID Medical, Inc.
- Category
- Medical Device — Surgical Kits
- Hazard
- Affected units
- 20
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- Model/Item Number (Kit): WRNM058-10
- UDI-DI: 10809160488898
- Kit Lot Numbers: 1681989
- Recalled Supplier Component (in kit): A902416
- Recalled Supplier Lot Number (in kit): NGKU2887
Distribution
Related recalls
Same manufacturer · AVID Medical, Inc.
See all →- ModerateAvid Medical Recalls Davinci Trucustom Bundles Due to Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls 23 ABD Hysterectomy Kits Due to Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls Plastic Trays Due to Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls Heart Prep Trays for Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination
FDA (Devices) · 2026-10-14
Same hazard · contamination
See all →- SevereCarolina Infusion Recalls Semaglutide Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereCarolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- ModerateAvid Medical Recalls Robotic Prostatectomy Packs for Lubricant Contamination
FDA (Devices) · 2026-10-14
- SevereFDA Recalls Tri-MIX Syringes Due to Sterility Assurance Concerns
FDA (Drugs) · 2026-10-14
Similar recalls
- ModerateAVID Medical Recalls Major Packs Due to Potential Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAvid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls 15 Laparoscopic Prostatectomy Kits for Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls GYN Laparoscopy Kits for Potential Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls Craniotomy Packs Due to Potential Lubricant Contamination
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination
FDA (Devices) · 2026-10-14