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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 4056140580 of 48,326 recalls

Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Zimmer, Inc.

Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...

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

Class II — Potential Health HazardOngoing
DrugJuly 16, 2014· Bio-pharm, Inc.

Recalled Item: Rugby Children's Pain and Fever Acetaminophen Oral Suspension 160 mg/5 mL...

The Issue: Superpotent Drug: Bio-Pharm, Inc. is initiating a recall of one lot of...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2014· Mars Food US

Recalled Item: Uncle Ben's(R) Ready Rice GARDEN VEGETABLE Recalled by Mars Food US Due to...

The Issue: Some pouches were filled with a different product that contains barley, a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 16, 2014· Market-Tiers Inc

Recalled Item: Instructions for Use for the blue endo MOREsolution Electromechanical...

The Issue: Some pages of the Instructions for Use were omitted, including pages...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension EXL Integrated Chemistry System in vitro diagnostic...

The Issue: The Reagent Lid hinge may lose its effectiveness and slowly shift downward...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· AGFA Healthcare Corp.

Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some sheets...

The Issue: Some sheets of the medical screen film are fogged.

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

Class III — Low RiskOngoing
Medical DeviceJuly 16, 2014· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs...

The Issue: Customers may receive positively biased results when using VITROS¿...

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

Class II — Potential Health HazardOngoing
DrugJuly 15, 2014· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 15, 2014· Vascutek, Ltd.

Recalled Item: Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a Recalled...

The Issue: The cautery that is provided with the Gelweave graft in the box has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Chemistry Wash (RD701) is an accessory of the Recalled by...

The Issue: Siemens Healthcare Diagnostics has received complaints for the Dimension...

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

Class II — Potential Health HazardOngoing
DrugJuly 14, 2014· Wockhardt Usa Inc.

Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by Wockhardt Usa Inc. Due to...

The Issue: Failed Impurities/Degradation Products: Out of specification levels of the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m) Recalled by Baxter...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/12.5 mg...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund