Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,836 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,836 in last 12 months

Showing 1668116700 of 27,852 recalls

Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2017· Zimmer Biomet, Inc.

Recalled Item: A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts Recalled...

The Issue: The drill guides were manufactured with the incorrect color anodization.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee Spacer Blocks To assist in partial knee Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the Persona Partial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Radio Capitellum Large Recalled by Howmedica Osteonics Corp. Due to Revision...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Standard Extended Stem Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: radial stem implant #2 (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Radiometer America Inc

Recalled Item: ABL800 analyzer with FLEXQ module. Device intended for in vitro Recalled by...

The Issue: Due to misinterpretation of the barcode by the scanner, when the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recon Extended Stem Size 2. Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recon Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp....

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: #2 Bipolar radial head Implant (Sterile packed). Orthopedic implant for...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: radial head implant #3 (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing