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. 2,426 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,426 in last 12 months

Showing 3430134320 of 51,038 recalls

DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Akorn, Inc.

Recalled Item: Sulfacetamide Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 16, 2016· Virtus Pharmaceuticals, Llc

Recalled Item: VP-CH-PNV Prenatal/Postnatal capsules Recalled by Virtus Pharmaceuticals,...

The Issue: Defective delivery system: Softgel capsules are leaking.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 16, 2016· FSC Laboratories, Inc

Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...

The Issue: Product had torn/loose seal around the mouthpiece.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...

The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2016· Medtronic Sofamor Danek Usa, Inc - Dallas Distribution

Recalled Item: Saw Sagittal Catalog Number: ES 300 Recalled by Medtronic Sofamor Danek Usa,...

The Issue: Medtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm...

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

Class II — Potential Health HazardOngoing
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: ARGININE 100MG/ML (PF) Recalled by Medaus, Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: HYDROGEN PEROXIDE 3% (PF) Recalled by Medaus, Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: M.I.C./B-COMPLEX (PF) B1-50MG Recalled by Medaus, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: GERMANIUM SESO 100MG/ML (PF) Recalled by Medaus, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: M.I.C 25/50/50 W/METHYL B12 1MG/PYRIDOXAL 50MG/ML (PF) Recalled by Medaus,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: FOLIC ACID 10MG/ML IN NACL (PF) Recalled by Medaus, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: LIPO-INJECTION W/LIDOCAINE (PF) Recalled by Medaus, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: NIACINAMIDE 100 MG/ML (PF) Recalled by Medaus, Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: LIPO-INJECTION W/LIDOCAINE NO METHIONINE W/PRES. (BENZYL ETOH 2%) ASCORBIC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund