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. 2,445 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,445 in last 12 months

Showing 2904129060 of 51,038 recalls

DrugJuly 6, 2017· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...

The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 6, 2017· Edwards Lifesciences, LLC

Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...

The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2017· HARDCORE FORMULATIONS

Recalled Item: D-ZINE Rapid Size and Strength capsules Recalled by HARDCORE FORMULATIONS...

The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 5, 2017· HARDCORE FORMULATIONS

Recalled Item: ULTRA-STEN Rapid Size and Strength capsules Recalled by HARDCORE...

The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 5, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension Recalled by Precision Dose Inc. Due to...

The Issue: Labeling Error: Label mix-up. Products' unit dose cups are correctly...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Builders Chocolate Mint 12-count Recalled by Clif Bar & Company Due to...

The Issue: Undeclared peanuts and/or tree nuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Kid Zbar Protein Chocolate Chip 10-pack Recalled by Clif Bar & Company...

The Issue: Undeclared peanuts and/or tree nuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Kid Zbar Protein Chocolate Mint 10-pack Recalled by Clif Bar & Company...

The Issue: Undeclared peanuts and/or tree nuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Builders Variety Pack Chocolate Peanut Butter and Chocolate Mint...

The Issue: Undeclared peanuts and/or tree nuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Kid Zbar Protein Variety Pack 30-count Recalled by Clif Bar & Company...

The Issue: Undeclared peanuts and/or tree nuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Raja Foods, L.L.C.

Recalled Item: Anarkali Peshawari Naan Bread Frozen 15oz. retail plastic pouch 24 Recalled...

The Issue: Undeclared milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2017· Cosman Medical, LLC

Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...

The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Roche Diagnostics Corporation

Recalled Item: cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number:...

The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Roche Diagnostics Corporation

Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...

The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Phadia US Inc

Recalled Item: Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command...

The Issue: The "Retry" command does not function properly which could cause a shortage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Novo Nordisk Inc

Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...

The Issue: A small number of batches may crack or break if exposed to certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Teleflex Medical

Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...

The Issue: Teleflex Medical is recalling the affected product because there may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· R82 A/S

Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...

The Issue: Replacement campaign on all units that have a gas spring head in aluminum.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Elekta, Inc.

Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...

The Issue: The table shift in the vertical direction was inverted during the use of CMA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing