Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,087 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,087 in last 12 months

Showing 11281–11300 of 51,038 recalls

Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM INDUSTRY COMBOURG LPT BROTH (4X3L) Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US Recalled by Biomerieux Inc Due...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: GENE-UP REAGENT GENE-UP LYSIS KIT Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL IMIPENEM IP 32 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PREVI COLOR GRAM REAGENT NOZZLE CLEANING SOLUTION (NA) Recalled by...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: API NIT1 NIT2 REAGENTS Recalled by Biomerieux Inc Due to As the temperature...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: BIOBALL A.BRASILIENSIS NCPF 2275 550X20 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL TOBRAMYCIN TM 256 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: BIOBALL K.RHIZOPHILA (30X20) Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· ENDO Pharmaceuticals Solutions, Inc.

Recalled Item: 9 Gauge Disposable Trocars with Blunt Pushers for Use with Recalled by ENDO...

The Issue: No expiration dates printed on the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Companion Medical, Inc.

Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...

The Issue: Diabetes management app may crash immediately upon opening, while using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...

The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...

The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Foundation Medicine, Inc.

Recalled Item: FoundationOne CDx (F1CDx) Recalled by Foundation Medicine, Inc. Due to...

The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Foundation Medicine, Inc.

Recalled Item: FoundationOne Liquid CDx (F1LCDx) Recalled by Foundation Medicine, Inc. Due...

The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2022· Getinge Usa Sales Inc

Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...

The Issue: The power backup battery, under certain conditions, may exhibit reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2022· Cordis US Corp

Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...

The Issue: There is a potential for separation at the male connector.

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

Class II — Potential Health HazardOngoing