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. 2,552 recalls have been distributed to Connecticut in the last 12 months.
Showing 15041–15060 of 51,038 recalls
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cubicin (daptomycin for injection) Recalled by MERCK SHARP & DOHME CORP Due...
The Issue: Presence of Particulate Matter: Identified as Glass Particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...
The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...
The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rizatriptan Benzoate Film Coated Tablets Recalled by MACLEODS PHARMA USA,...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 10mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 5mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...
The Issue: A potential risk for false negative nitrite results exists when endogenous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Western Oxytote DTE Digital VIPR System (with D-size cylinder) Model:...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Western Oxytote DTE Digital VIPR System (with E-size cylinder) Model:...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roberts Digital VIPR System (with E-size cylinder) Model: ROC-9840 Recalled...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600 Recalled by...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Udel Sterilization Tray Instructions for Use Recalled by Karl...
The Issue: To ensure sterilization effectiveness, sterilization tray instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.