RecallRadar

FDA Device recall Z-0097-2027

PACK OPEN HEART CFH

On 2026-10-14 the FDA classified a Class II recall of PACK OPEN HEART CFH 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-0097-2027
ClassificationClass II
Statusongoing
Initiated2026-08-10
Published2026-10-14
Last updated2026-10-21 05:30 UTC
CompanyAvid Medical
DistributionUS

Product

PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;

Reason

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

Identifiers

code_info
1. Model/Item Number (Kit): UFCF004-06; UDI-DI: 10809160487334; Kit Lot Numbers: 1666214, 1672814; 2. Model/Item Numbe…1. Model/Item Number (Kit): UFCF004-06; UDI-DI: 10809160487334; Kit Lot Numbers: 1666214, 1672814; 2. Model/Item Number (Kit): UFCF004-07; UDI-DI: 10809160513170; Kit Lot Numbers: 1695181; Recalled Supplier Component (in kit): A119216M; Recalled Supplier Lot Number (in kit): NGKT2404, NGKT3314;

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-0097-2027%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.