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. 956 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
956 in last 12 months

Showing 36101–36120 of 48,326 recalls

Medical DeviceJuly 22, 2015· Beckman Coulter Inc.

Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...

The Issue: The end cap may loosen and detach making the instrument non-functional. No...

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

Class II — Potential Health HazardOngoing
FoodJuly 22, 2015· Samuel Adams Brewery Co

Recalled Item: Apple Orchard Crisp Apple Hard Cider Three packages sizes: ¿ Recalled by...

The Issue: Due to concerns of re-fermentation, bottles may burst under increased pressure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2015· Wright Medical Technology, Inc.

Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...

The Issue: These screws have a potential of passing through the plate in the case when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2015· Wright Medical Technology, Inc.

Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...

The Issue: These screws have a potential of passing through the plate in the case when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2015· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...

The Issue: Channel Error code is displayed on the PC unit with an audio and visual...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 21, 2015· Neuro Kinetics, Inc.

Recalled Item: Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that...

The Issue: The devices that included the OVAR research test were not cleared for...

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

Class II — Potential Health HazardOngoing
DrugJuly 21, 2015· Apotex Inc.

Recalled Item: Verapamil Hydrochloride Extended-Release tablets Recalled by Apotex Inc. Due...

The Issue: Failed Dissolution Specification: One lot of product did not meet the first...

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

Class III — Low RiskOngoing
Refund
DrugJuly 21, 2015· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Phentermine Hydrochloride Capsules Recalled by PD-Rx Pharmaceuticals, Inc....

The Issue: Failed impurities/Degradation specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugJuly 20, 2015· Qualitest Pharmaceuticals

Recalled Item: ALLOPURINOL TABLETS Recalled by Qualitest Pharmaceuticals Due to Failed...

The Issue: Failed Tablet/Capsule Specifications; report of oversized and discolored tablets

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 20, 2015· Trilliant Surgical Ltd.

Recalled Item: Concave Reamer Head Recalled by Trilliant Surgical Ltd. Due to The...

The Issue: The cannulation of the Concave and Convex Reamer Heads may be too small to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2015· Trilliant Surgical Ltd.

Recalled Item: Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE Recalled by...

The Issue: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2015· Trilliant Surgical Ltd.

Recalled Item: 3.0/4.0 Cannulated Drill Bit Recalled by Trilliant Surgical Ltd. Due to The...

The Issue: The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 2 Waste Management System Docking Station (120V and 230V) Recalled...

The Issue: The Fluid Coupling Sleeve, a component within the Neptune Waste Management...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2015· Trilliant Surgical Ltd.

Recalled Item: 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and...

The Issue: The cutting efficiency of the Countersinks was out of specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2015· GE Healthcare

Recalled Item: PET Discovery LS Recalled by GE Healthcare Due to Potential for expulsion of...

The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2015· Advanced Sterilization Products

Recalled Item: Wall Chart for STERRAD 100NX System Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2015· Medtronic Navigation, Inc.

Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....

The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2015· GE Healthcare

Recalled Item: Lightspeed 16 CT Recalled by GE Healthcare Due to Potential for expulsion of...

The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2015· Medtronic Navigation, Inc.

Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....

The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...

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

Class II — Potential Health HazardOngoing