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. 2,349 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,349 in last 12 months

Showing 3416134180 of 48,326 recalls

Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: PRCT MIS CR MOB PLT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: Metasul Head 40 Recalled by Zimmer Biomet, Inc. Due to LDPE bag containing...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Varian Medical Systems, Inc.

Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...

The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro Recalled by Horiba...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Glucose PAP CP ref. A11A01668 reagent is intended Recalled by...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic Recalled...

The Issue: Blade exhibiting fracture during hip arthroscopy procedures

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: VERSYS 6 INCH BEADED FC 1 prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: CR Flex GSF Porous Femoral LPS Flex GSF Porous Femoral Recalled by Zimmer...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Medtronic Neuromodulation

Recalled Item: Specify 5-6-5 Lead Recalled by Medtronic Neuromodulation Due to Some Specify...

The Issue: Some Specify 5-6-5 and 2x8 surgical lead product labeling does not...

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

Class II — Potential Health HazardOngoing
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Stree Overlord Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Zhong Hua Niu Bian Recalled by R Thomas Marketing, LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Germany Niubian Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Herb Viagra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bigger Longer More Time More Sperms Recalled by R Thomas Marketing, LLC Due...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Super Hard Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: African Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund