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. 2,443 recalls have been distributed to Montana in the last 12 months.
Showing 19641–19660 of 48,326 recalls
Recalled Item: Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement Recalled...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...
The Issue: Sterile packaging incomplete seals may compromise sterility of the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.