Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 27041–27060 of 48,219 recalls
Recalled Item: Major Ferrous Drops Recalled by The Harvard Drug Group Due to The...
The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...
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: Rugby Tri-vitamin Liquid Recalled by The Harvard Drug Group Due to The...
The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...
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 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: 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 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: 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: 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 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: 140" (356 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: 88" (224 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: 99" (251 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: 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: 120" (305 cm) 10 Drop Primary Set w/2 MicroClave¿ 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: 94" (239 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: 112" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...
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.