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. 1,039 recalls have been distributed to Montana in the last 12 months.
Showing 15061–15080 of 48,326 recalls
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...
The Issue: Claim for stability after reconstitution from lyophilized to liquid form...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...
The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Double Chocolate Plant-Based Protein Shake Recalled by Pepsico Inc...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Vanilla Bean Plant-Based Protein Shake Recalled by Pepsico Inc Due to...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic CB10W64R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hays Ultrasound kit Item ID: H1000SE Recalled by Exact Medical...
The Issue: No 510k for the product to be used in a natural or surgical opening to the body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...
The Issue: No 510k for the product to be used in a natural or surgical opening to the body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8M63R4 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB1H18R20 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY7M07R6 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 1A46R11 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10R55R5 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.