Remel Inc Recalls

FDA
41
Total Recalls
1
Agencies
Jul 2008
First Recall
Sep 2024
Latest Recall

Showing 41-41 of 41 recalls

FDA

Remel RapID Inoculation Fluid, Microorganism differentiation and identification device, Packaged in 1-ml tube, Catalog Number: R8325102, 20/pack, Remel, Lenexa, KS 66215

Failure to produce reaction: Use of the product with various RapID Identification systems panels may exhibit poor or no reactions.

Consignees were notified by an Important Medical Device Customer Advisory Notice on 10/23/07. The letter instructs users to review inventory and discard any affected products. The letter also instructs users to return a product inventory checklist by 11/23/07. For additional information, contact 1-800-447-3641.