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. 2,542 recalls have been distributed to Montana in the last 12 months.
Showing 5721–5740 of 48,326 recalls
Recalled Item: Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion Recalled by ARG...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syringes labeled as: a) SYR 10ML L/L CONTROL Recalled by MEDLINE INDUSTRIES,...
The Issue: These syringes were identified to be affected by the FDA Safety Alert issued...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pump Rotor Recalled by Fresenius Medical Care Holdings, Inc. Due to An...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial access kit (without Prep solutions) Bit and Guard- Recalled...
The Issue: Potential holes and tears in the sterile packaging (header bag) of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Inspection System Recalled by YAMAHA MOTOR CORPORATION Due to...
The Issue: Non-medical laser products which were determined to not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yamaha Surface Mounter YR series Recalled by YAMAHA MOTOR CORPORATION Due to...
The Issue: Non-medical laser products which were determined to not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syntel Silicone Thrombectomy Catheter Recalled by LeMaitre Vascular, Inc....
The Issue: The guide tip can become damaged and result in the tip detaching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in....
The Issue: Potential contamination of the product with latex adhesive residual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelli-C: Right side suspended Tabletop Recalled by NRT X-RAY A/S Due to...
The Issue: X-ray system C-arm may experience uncontrolled motion if 1) AC motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA MRI S VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT DR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT DR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT XT VR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRRO MRI VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.