MINC+ Benchtop Incubator — Class II medical device recall Z-0722-2024
Ongoing recall by Cook Medical Llc, reported 2024-01-24, distributed in CA, IN, LA, MD, NY. The MINC+ device is susceptible to losing temperature control of electrostatic discharge (static electricity)
| Recall number | Z-0722-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Medical Llc, Bloomington, IN, United States |
| Recall initiated | 2023-12-07 |
| Classified | 2024-01-12 |
| Reported by FDA | 2024-01-24 |
| Distributed | CA, IN, LA, MD, NY |
| Countries outside the US | AT, AU, CH, ES, FI, FR, GB, IE, IN, IT, KW, TR |
| Reason classes | temperature control |
| UPC / GTIN / UDI-DI | 00827002444294 |
| Lot numbers | AM109356, AM109363, AM109365, AM111932, AM111933, AM111934, AM112039, AM112040, AM112041, AM112042, AM112043, AM112071, AM112072, AM112316 |
| Model numbers | K-MINC-2000 |
Product
MINC+ Benchtop Incubator, Reference Part Number (RPN) K-MINC-2000, Order Number (GPN) G44429
Reason for recall
The MINC+ device is susceptible to losing temperature control of electrostatic discharge (static electricity) is applied to the lid of the device. This may lead to embryo degeneration necessitating an additional medical procedure for the patient.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0722-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.