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.

51,038 total recalls
2,485 in last 12 months

Showing 2074120760 of 51,038 recalls

DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Akorn, Inc.

Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...

The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Grato Holdings, Inc.

Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...

The Issue: Labeling mix-up - Indications on product label are incorrect.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 14, 2019· Cardinal Health Inc.

Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....

The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Cardinal Health Inc.

Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...

The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Cardinal Health Inc.

Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...

The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Abbott Diabetes Care, Inc.

Recalled Item: Precision Xtra Blood Glucose & Ketone Monitoring System Recalled by Abbott...

The Issue: Instructions sent in a letter or in instructions for use for disinfecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Abbott Diabetes Care, Inc.

Recalled Item: Optium EZ Blood Glucose Monitoring System Recalled by Abbott Diabetes Care,...

The Issue: Instructions sent in a letter or in instructions for use for disinfecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Precision H Blood Glucose and Ketone Monitoring System Recalled by...

The Issue: Instructions sent in a letter or in instructions for use for disinfecting...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2019· Natures Rx

Recalled Item: Silver Bullet Recalled by Natures Rx Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2019· Precision Dose Inc.

Recalled Item: Ranitidine Oral Solution Recalled by Precision Dose Inc. Due to CGMP...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 13, 2019· GETINGE US SALES LLC

Recalled Item: Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion...

The Issue: Sterile barrier system may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2019· Linet Spol. S.r.o.

Recalled Item: Eleganza 5 (AC powered adjustable bed) Recalled by Linet Spol. S.r.o. Due to...

The Issue: A component used within the side rail mechanism may malfunction, resulting...

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

Class II — Potential Health HazardOngoing
DrugNovember 12, 2019· Integrated Health Concepts Inc. dba Conversio Health

Recalled Item: Albuterol 2.5mg / Ipratropium 0.75mg /Budesonide 0.5mg Recalled by...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· Integrated Health Concepts Inc. dba Conversio Health

Recalled Item: Budesonide 0.4mg Recalled by Integrated Health Concepts Inc. dba Conversio...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund