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 26701–26720 of 48,219 recalls
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Death Wish Nitro Canned Cold Brew Coffee 11 oz Recalled by Death Wish Coffee...
The Issue: Potential for Clostridium Botulinum
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 Recalled by...
The Issue: Outer box fails to declare the allergen walnuts, the individual bar is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bio35 Recalled by Pro Bioteks Laboratories Due to Undeclared Soy
The Issue: Bio-35 has undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RHINO 7 Platinum 5000 Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intralipid 20% Recalled by Baxter Healthcare Corporation Due to Temperature...
The Issue: Temperature Abuse: A portion of this product lot was exposed to subfreezing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminocaproic Acid Recalled by Medisca, Inc. Due to CGMP Deviations: Product...
The Issue: CGMP Deviations: Product manufactured for Industrial Use but was labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of...
The Issue: Presence of particulate matter: glass flakes identified as lamellae observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.