Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,602 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
1,602 in last 12 months

Showing 54215440 of 27,655 recalls

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: 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: 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· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPOINT 500e 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 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· 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: 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: TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV Recalled by B. Braun Medical, Inc....

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 25, 2023· Securitas Healthcare LLC

Recalled Item: Arial Water Resistant Pendant with Long Wristband Recalled by Securitas...

The Issue: Premature battery depletion presents a risk that alarms will not be received...

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: Hysteroscope-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· Encore Medical, LP

Recalled Item: RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm Recalled by...

The Issue: Two different humeral socket Insert devices were swapped during packaging,...

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: 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: 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: Uretero-reno fiberscope-For endoscopic diagnosis and treatment 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: 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: 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: 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: 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