Radiomat M+ NIF 14 x 17 recall
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…
Why was Radiomat M+ NIF 14 x 17 recalled?
Some sheets of the medical screen film are fogged.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Batch No. 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…
- Recalling firm
- AGFA Healthcare Corp.
- Quantity
- 2617
- Distribution
- Worldwide Distribution and US Nationwide in the states of AL, AZ, CA, FL, IL, LA, MI, MN, MS, NE, NH, NJ, NC and country of Canada
- Recall date
- August 20, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)