Radiomat M+ NIF 14 x 17 — Class III medical device recall Z-2178-2014
Terminated recall by AGFA Healthcare Corp., reported 2014-08-20, distributed nationwide. Some sheets of the medical screen film are fogged.
| Recall number | Z-2178-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AGFA Healthcare Corp., Greenville, SC, United States |
| Recall initiated | 2014-07-16 |
| Classified | 2014-08-09 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2014-12-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 2,617 |
| Lot numbers | 79350052, 79380052, 79390074, 79400066, 79410063 |
Product
Radiomat M+ NIF 14 x 17; Radiomat SG 14 x 17 NIF; RX-B 8 x 10 in./IBF-004355; Radiomat B+ NIF 14 x 17; Radiomat B+ NIF 8 x 10; Radiomat B+ NIF 9 1/2 x 9 1/2; CX Ultra UV-G Plus NIF 11 x 14; Radiomat G Plus 14 x 17 NIF Product Usage: Radiographic film is a device that consists of a thin sheet of radiotransparent material coated on one or both sides of the film, with a radiotransparent material coated on one or both sides of the film, with a photographic emulsion intended to record images during diagnostic radiologic procedures.
Reason for recall
Some sheets of the medical screen film are fogged.
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-2178-2014. 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.