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. 2,485 recalls have been distributed to Connecticut in the last 12 months.
Showing 20701–20720 of 51,038 recalls
Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...
The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamb Weston Grown In Idaho Crispy Hash Brown Dices Recalled by Lamb Weston...
The Issue: Crispy Hash Brown Dices product is recalled because it may contain pieces of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 8 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 7 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Introducer Sets Maquet 7.5 Fr. Recalled by Datascope Corporation...
The Issue: Potential for compromised sterility in breached pouches of specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...
The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...
The Issue: Lack of Assurance of Sterility: Product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...
The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product...
The Issue: Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...
The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.