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. 2,284 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,284 in last 12 months

Showing 4312143140 of 48,326 recalls

Medical DeviceSeptember 11, 2013· ArjoHuntleigh Inc.

Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...

The Issue: The lock pin can become stuck in the "in" position during the manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Harvest Technologies Corporation

Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...

The Issue: Potential for leur connector to leak or have cracks.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· SonoSite, Inc.

Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...

The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Steris Corporation

Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...

The Issue: STERIS has identified that the population of the G. stearothermophilus...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Aesculap, Inc.

Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...

The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Wexford Labs Inc

Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...

The Issue: Expired active ingredient was used in the manufacture of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Baxter Healthcare Corp.

Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...

The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Integra Limited

Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...

The Issue: Integra LifeSciences has identified through an internal evaluation that in...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Bevacizumab 1.25 mg/0.05 mL PF Recalled by Avella of Deer Valley, Inc. Due...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund