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. 2,535 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,535 in last 12 months

Showing 74617480 of 48,219 recalls

Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: 30ML BURETTE ASSY WITH STOPCOCK Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: ALLERGAN UNIVERSAL FILL KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: FT1000S FLUID TRANSFER SET Recalled by B. Braun Medical, Inc. Due to Devices...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: SA3000 VENTED MICRO SPIKE ADAPTER Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: BULK LARGEBORE MALE LL FITTING Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2023· Scynexis, Inc.

Recalled Item: BREXAFEMME (Ibrexafungerp) tablets 150 mg Recalled by Scynexis, Inc. Due to...

The Issue: Cross Contamination with Other Products: Potential cross-contamination of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 25, 2023· Penzeys, Ltd.

Recalled Item: Penzeys Brady Street Cheese Sprinkle. Item 20756. net wt 2.2 Recalled by...

The Issue: Brady Street Cheese Sprinkle may contain sesame.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2023· Olympus Corporation of the Americas

Recalled Item: Insufflation unit Recalled by Olympus Corporation of the Americas Due to...

The Issue: Olympus has become aware of an increased trend of both repairs and customer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Tracheal fiberscope-airway management Recalled by Aizu Olympus Co., Ltd. Due...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA)...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Choleodochoscope. Model Numbers: CHF-BP30 Recalled by Aizu Olympus Co., Ltd....

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Bronchoscope-for endoscopy and endoscopic surgery within the airways and...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Colonoscope-indicated for use within the lower digestive tract (including...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging Recalled...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Ureteralscope- for endoscopic diagnosis and treatment within the ureter...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Cystonephroscope-endoscopic diagnosis and treatment within the bladder...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Tracheal videoscope- For airway management Recalled by Aizu Olympus Co.,...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing