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. 2,034 recalls have been distributed to Wyoming in the last 12 months.
Showing 3221–3240 of 48,219 recalls
Recalled Item: Allura Xper FD20/20 System Code: (1) 722038 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 Recalled...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C System Code: (1) 722001 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monkey Spit "Swamp Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...
The Issue: Barbeque sauce product contains undeclared allergens (soy) contained in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monkey Spit "Atomic Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...
The Issue: Barbeque sauce product contains undeclared allergen listing of (Milk) in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monkey Spit "Monkey Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...
The Issue: Barbeque sauce product contains undeclared listing of (Milk) in product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by The Harvard Drug Group...
The Issue: CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL Recalled by Teva...
The Issue: Failed Stability Specifications - 12-month stability test result for one of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...
The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...
The Issue: Due to manufacturing issue (unintended by-product of the injection molding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing device labeling is being updated to strengthen labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...
The Issue: Potential that the induction seal is not completely sealed to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...
The Issue: Product complaints were received describing the A820 myPTM app taking longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.