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 3052130540 of 51,038 recalls

FoodApril 27, 2017· Lords Organics Llc

Recalled Item: Organic Veda brand Ginger Powder Recalled by Lords Organics Llc Due to...

The Issue: Lord Organics is recalling ginger powder because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 27, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for peel force from the...

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2017· Hetero USA Inc

Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...

The Issue: Presence of Foreign Substance: human hair melded into tablet.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 26, 2017· Iba Dosimetry

Recalled Item: Large Stealth Chamber Recalled by Iba Dosimetry Due to When the Stealth...

The Issue: When the Stealth Chamber is used as a detector in relative dosimetry,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2017· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffmann LRF Safety Clip (Bone Transport Strut) Recalled by Stryker...

The Issue: Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety...

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

Class II — Potential Health HazardOngoing
FoodApril 26, 2017· Rich Products Corp

Recalled Item: 7 OZ PIZZA DOUGH BALL Recalled by Rich Products Corp Due to Potential E....

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and...

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: ARTISAN CRUST PIZZA DOUGH 24/18 Recalled by Rich Products Corp Due to...

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 25, 2017· Vascular Solutions, Inc.

Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...

The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Bard Access Systems Inc.

Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...

The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Endoscopic Introducer/Extractor Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· BioMerieux SA

Recalled Item: ETEST ETP32 (Ertapenem) Ref. 531640 Recalled by BioMerieux SA Due to False...

The Issue: False susceptible results

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Pereyra Ligature Carrier 75 Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Clarke-Reich Laparoscopic Knot Pusher Recalled by Cook Inc. Due to...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Beckman Coulter Inc.

Recalled Item: Microalbumin Reagent Recalled by Beckman Coulter Inc. Due to Beckman Coulter...

The Issue: Beckman Coulter has confirmed that MA Reagent Lot M609458 may recover...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: There is a possibility of a data acquisition disruption that may cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: There is a possibility of a data acquisition disruption that may cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2017· Molnlycke Health Care, Inc

Recalled Item: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin...

The Issue: Sterilization validation failure.

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

Class II — Potential Health HazardOngoing