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. 1,074 recalls have been distributed to Connecticut in the last 12 months.
Showing 15861–15880 of 51,038 recalls
Recalled Item: Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron CX/DX/LX Beta-Hydroxybutyrate . in vitro diagnostic reagent....
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System . An automated immunoassay analyzer for Recalled by Abbott...
The Issue: A design defect (hardware and software) allows liquid waste pressure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Now Real Food Organic Steel Cut Oats Recalled by NOW Health Group Inc. Due...
The Issue: Specific lot of Organic Steel Cut Oats, may actually contain Organic Beet Sugar
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)) Recalled by NATIVE PROMOTIONS,...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Compounded Lyophilized Semorelin/Ipamorelin 3 mg For subcutaneous or...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Compounded Lyophilized AOD-9604 Recalled by Innoveix Pharmaceuticals Inc Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COPAN FLOQSwabs Recalled by Copan Italia Due to A sterility assurance level...
The Issue: A sterility assurance level of 10-6 cannot be guaranteed due to intentional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUABEAM Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to Scope...
The Issue: Scope tube tip may detach from the telescoping tube, which is attached to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUL8 LUXE DVT PREVENTION DEVICE Recalled by Ortho8, Inc. Due to CIRCUL8...
The Issue: CIRCUL8 LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVEXIA LUXE DVT PREVENTION DEVICE Recalled by Ortho8, Inc. Due to EVEXIA...
The Issue: EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX Recalled...
The Issue: Due to failure to acquire pre-market clearance for its high resolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to The seating system...
The Issue: The seating system unexpectedly detached, which resulted in the seating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to The seating system...
The Issue: The seating system unexpectedly detached, which resulted in the seating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpion Portal Vein Access Set - Product Usage: used to Recalled by Argon...
The Issue: As a result of design changes, sheaths have exhibited cracking/breaking at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dose IQ Safety Software used with Spectrum IQ Infusion Pump Recalled by...
The Issue: Software issue: The defect creates a mismatch between linked drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Aurobindo Pharma USA...
The Issue: Presence of Foreign Substance- Potential of metal contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Dx 100 Blood Collection Card Quantity 25 Recalled by Advance Dx,...
The Issue: Due to high glucose test results when using the blood collection cards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM BR 27.29 (BR) Assay 250 Test Kit ()- Recalled by Siemens...
The Issue: Product does not meet the Instructions for Use (IFU) claimed Pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM BR 27.29 (BR) Assay 50 Test Kit- in Recalled by Siemens...
The Issue: Product does not meet the Instructions for Use (IFU) claimed Pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.