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.
Showing 43781–43800 of 48,326 recalls
Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nata Komplete Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NataChew Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 430 ec Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 430 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS Recalled by Priester...
The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PRIESTER'S PECANS brand FANCY ROASTED NUTS Recalled by Priester Pecan...
The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PRIESTER'S PECANS brand NUTTY FAVORITES ASST Recalled by Priester Pecan...
The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vinco's OsteoSheath 4 Enhanced Bone Support Recalled by Vinco Inc. Due to...
The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vinco's Fem-Vite Women's Anti-Oxidant Formula Recalled by Vinco Inc. Due to...
The Issue: The soy ingredient used to manufacture certain lots of Vinco's Fem-Vite was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vinco's OsteoSheath Enhanced Bone Support Recalled by Vinco Inc. Due to...
The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...
The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...
The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...
The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.