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. 2,498 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,498 in last 12 months

Showing 1296112980 of 48,326 recalls

Medical DeviceFebruary 2, 2022· Philips North America Llc

Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...

The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2022· Ace Surgical Supply Co., Inc.

Recalled Item: NuOss Collagen Block Size 8mm x 9mm x 9mm- used Recalled by Ace Surgical...

The Issue: NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BSN Medical Inc

Recalled Item: (1) JOBST Compri2 Recalled by BSN Medical Inc Due to Mislabeling

The Issue: The folding boxes within the shipping case are mislabeled. The shipping case...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· Mevion Medical Systems, Inc.

Recalled Item: Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N Recalled by...

The Issue: Malfunction of the hand pendant controlling movement of the therapy couch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· Canon Medical System, USA, INC.

Recalled Item: INFX-8000V. For radiographic and fluoroscopic studies and intervention....

The Issue: The fluoroscopic dose rate might exceed the conforming value during biplane...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Ysiosystem with VC10 software version Recalled by Siemens Medical Solutions...

The Issue: Siemens Healthineers has identified a software error in previous software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· SD Biosensor, Inc.

Recalled Item: STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Recalled by SD...

The Issue: Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 31, 2022· B. Braun Medical, Inc.

Recalled Item: Dispensing Pins for Air Inlet Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: This lot may have an elevated risk of leakage from the Air-Inlet Filter of...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 28, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund