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. 1,043 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,043 in last 12 months

Showing 14101–14120 of 48,326 recalls

DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Fulvestrant Injection 250 mg/5 mL (50 mg/mL) For Intramuscular Use Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules USP 50 mg 100 Capsules Rx Only NDC Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF Recalled by DuPont...

The Issue: Microbial Contamination of Non-Sterile Product: Out-of-specification results...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 26, 2021· AVRIO HEALTH L.P

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by AVRIO...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 26, 2021· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Atrium Medical Corporation

Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...

The Issue: The product package may potentially contain a mismatched graft that does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Accelerated Care Plus Corporation

Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing