Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,111 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,111 in last 12 months

Showing 5521–5540 of 29,298 recalls

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
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: 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: 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: 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: AMO ADMINISTRATION SET Recalled by B. Braun Medical, Inc. Due to Devices may...

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: 30 ML 2PORT BURETTE ASSEMBLY 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: THERASPHERE ADMIN SET Recalled by B. Braun Medical, Inc. Due to Devices may...

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· PATH

Recalled Item: SENTIERO Recalled by PATH Due to Affected lots of product may experience...

The Issue: Affected lots of product may experience technical distortions to a greater...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· PATH

Recalled Item: SENTIERO Screening2 Recalled by PATH Due to Affected lots of product may...

The Issue: Affected lots of product may experience technical distortions to a greater...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPOINT 500 Blood Gas System Recalled by Siemens Healthcare Diagnostics...

The Issue: There are potential drug interferences from Perhexiline Maleate or...

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: Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number:...

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: Small intestinal videoscope-For endoscopy and endoscopic surgery within the...

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: 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: Colonoscope: for endoscopy and endoscopic surgery within the lower digestive...

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: Ultrasonic gastrovideoscope-Real time ultrasound imaging Recalled by Aizu...

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: Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps)...

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