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. 2,271 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,271 in last 12 months

Showing 4686146880 of 48,326 recalls

Medical DeviceAugust 3, 2012· Instrumentation Laboratory Co.

Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...

The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2012· Newport Medical Instruments Inc

Recalled Item: Newport HT70 and HT70 Plus Ventilators Recalled by Newport Medical...

The Issue: May emit a continuous high priority alarm and the ventilator may stop...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 3, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: The Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The patient support may move in an unintended manner if the foot switch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2012· Medical Specialties Distributors, Inc.

Recalled Item: Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration...

The Issue: Devices leaking at the Y-site

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

Class II — Potential Health HazardOngoing
FoodAugust 2, 2012· Deep Foods Inc

Recalled Item: Crispy Punjabi Cookies Recalled by Deep Foods Inc Due to This recall has...

The Issue: This recall has been initiated due to Non-Declared Milk. This product may...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 2, 2012· Kreg Medical Inc.

Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...

The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2012· Hospira, Inc.

Recalled Item: Sterile Empty Vial and Injector (30mL PCA vial) Recalled by Hospira, Inc....

The Issue: Reports of leaking during filling and administration.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2012· Steris Corporation

Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...

The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2012· Phadia US Inc

Recalled Item: PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test...

The Issue: Customers were not following the labeled assay procedure. This was due to a...

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

Class III — Low RiskOngoing
DrugAugust 1, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Chemical Contamination: The product is being recalled due to complaints...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Chemical Contamination: The product is being recalled due to complaints...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Chemical Contamination: The product is being recalled due to complaints...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· Steris Corporation

Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...

The Issue: The firm initiated a recall after complaint investigations revealed that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...

The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2012· Respironics California Inc

Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...

The Issue: Respironics is recalling the V60 ventilator because certain blower motor...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2012· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...

The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...

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

Class II — Potential Health HazardOngoing
DrugJuly 30, 2012· Genentech Inc

Recalled Item: Trastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg)...

The Issue: Presence of Particulate Matter: One lot of Bacteriostatic Water for...

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

Class I — Serious Health HazardOngoing
Refund