Z-0104-2027 Class II Ongoing
FDA device recall Z-0104-2027 was initiated by AVID Medical, Inc. on Aug 10, 2026 and is designated Class II. Reason for recall: Product may be potentially contaminated with a lubricant used during the manufacturing process. The recall status is ongoing. Affected quantity: 40.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 14, 2026
- Initiation Date
- Aug 10, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 40
Product Description
MAJOR PACK; Model/Item Number (Kit): NIHB0018-11;
Reason for Recall
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Distribution Pattern
US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
Code Information
Model/Item Number (Kit): NIHB0018-11; UDI-DI: 10809160403747; Kit Lot Numbers: 1667763; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKT3375;
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0104-2027
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026