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. 2,408 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,408 in last 12 months

Showing 3818138200 of 51,038 recalls

Medical DeviceJuly 15, 2015· Iris Diagnostics

Recalled Item: iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049 Recalled by...

The Issue: Iris International is recalling the iChemVELOCITY systems because they do...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ CREA (Creatinine) and Dimension Vista¿ CREA (Creatinine) Recalled...

The Issue: Siemens has confirmed that the Dimension CREA and Dimension Vista CREA may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2015· Medtronic Cardiovascular Surgery-the Heart Valve Division

Recalled Item: EnVeo R Loading System Recalled by Medtronic Cardiovascular Surgery-the...

The Issue: Medtronic is recalling the EnVeo R Loading Systems because of the presence...

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

Class I — Serious Health HazardOngoing
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: biotene Gentle Formula FLUORIDE TOOTHPASTE Fresh Mint Original Recalled by...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: biotene Gentle Mint Gel Recalled by GlaxoSmithkline Consmer Healthcare Due...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: SENSODYNE EXTRA FRESH REPAIR & PROTECT Recalled by GlaxoSmithkline Consmer...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: SENSODYNE EXTRA FRESH COMPLETE PROTECTION Recalled by GlaxoSmithkline...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: SENSODYNE COMPLETE PROTECTION Recalled by GlaxoSmithkline Consmer Healthcare...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: biotene PBF Toothpaste (Plaque-Biofilm Loosening Formula) Recalled by...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: biotene Gentle Formula FLUORIDE TOOTHPASTE GENTLE MINT Recalled by...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2015· GlaxoSmithkline Consmer Healthcare

Recalled Item: SENSODYNE WITH FLUORIDE REPAIR & PROTECT Recalled by GlaxoSmithkline Consmer...

The Issue: Presence of Foreign Substance: Fragments of wood found when the product was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2015· KVK-Tech, Inc.

Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK-Tech, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 14, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: cobas b 123 Fluid Pack COOX 400 Product Recalled by Roche Diagnostics...

The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: cobas b 123 Fluid Pack COOX 200 Product Recalled by Roche Diagnostics...

The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....

The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....

The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Draeger Medical, Inc.

Recalled Item: PS500 of an IACS Workstation Critical Care (Evita Infinity V500) Recalled by...

The Issue: The battery capacity of the optional PS500 of an IACS Workstation Critical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Sedecal S.A.

Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....

The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...

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

Class II — Potential Health HazardOngoing
DrugJuly 13, 2015· Purdue Pharma L.P.

Recalled Item: Intermezzo (zolpidem tartrate) Recalled by Purdue Pharma L.P. Due to Failed...

The Issue: Failed dissolution specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJuly 13, 2015· Perrigo Israel Pharmaceuticals

Recalled Item: Mometasone Furoate Ointment USP Recalled by Perrigo Israel Pharmaceuticals...

The Issue: Subpotent drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund