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. 2,359 recalls have been distributed to Montana in the last 12 months.
Showing 27441–27460 of 48,326 recalls
Recalled Item: Amrita Mango Coconut Energy Bar Recalled by Amrita Health Foods Due to...
The Issue: Product may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amrita Apple Cinnamon Energy Bar Recalled by Amrita Health Foods Due to...
The Issue: Product may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amrita Pineapple Chia Energy Bar Recalled by Amrita Health Foods Due to...
The Issue: Product may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amrita Dark Chocolate Quinoa 15g Protein Bar Recalled by Amrita Health Foods...
The Issue: Product may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amrita Sunflower Butter & Jelly 15g Protein Bar Recalled by Amrita Health...
The Issue: Product may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amrita Apricot Strawberry Protein Bar Recalled by Amrita Health Foods Due to...
The Issue: Product may be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NATURAL HERBAL COFFEE AMPT Recalled by The Ampt Life, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Presource(R) Kits (custom surgical/procedural kits): The standard and custom...
The Issue: The firm manufactured and distributed Presource(R) kits which contained BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Recalled by Zimmer Biomet, Inc. Due to The products...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled Recalled by...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Tray Triple Lumen Polyurethane Catheter Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM...
The Issue: The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Tray Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 121" (307 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 120" (305cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 143" (363 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 128" (325 cm) Y-Type Blood Set with 170 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.