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. 2,472 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,472 in last 12 months

Showing 2164121660 of 51,038 recalls

DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2019· Ra Medical Systems, Inc.

Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...

The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2019· Philips North America, LLC

Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...

The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...

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

Class II — Potential Health HazardOngoing
FoodAugust 22, 2019· Great One Trading Inc.

Recalled Item: QQ Fish brand Mushroom Fish Ball Recalled by Great One Trading Inc. Due to...

The Issue: Products contain undeclared allergen, specifically egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 22, 2019· Great One Trading Inc.

Recalled Item: QQ Fish brand Tofu Style Fried Fish Cake Recalled by Great One Trading Inc....

The Issue: Products contain undeclared allergen, specifically egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 22, 2019· Great One Trading Inc.

Recalled Item: QQ Fish brand CUTTLEFISH FLAVOURED SEAFOOD BALL Recalled by Great One...

The Issue: Product contains an undeclared allergen, specifically egg, that is not...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 22, 2019· Great One Trading Inc.

Recalled Item: QQ Fish brand SHRIMP FLAVOURED SEAFOOD BALL Recalled by Great One Trading...

The Issue: Product contains an undeclared allergen, specifically egg, that is not...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 22, 2019· Great One Trading Inc.

Recalled Item: QQ Fish brand CRAB FLAVOURED SEAFOOD BALL Recalled by Great One Trading Inc....

The Issue: Product contains an undeclared allergen, specifically egg, that is not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2019· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Concerto & Basic Shower Trolly Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....

The Issue: The firm has become aware that any of the 4 safety catches may exhibit a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2019· LivaNova USA Inc

Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...

The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 22, 2019· Thoratec Switzerland GMBH

Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...

The Issue: Reports have been received of the CentriMag Systems experiencing motor and...

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

Class I — Serious Health HazardOngoing
DrugAugust 21, 2019· Macleods Pharma Usa Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...

The Issue: Subpotent Drug: Out of specification result during stability study in...

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2019· Seattle Gourmet Foods Inc.

Recalled Item: FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a...

The Issue: FungusAmongUs Shiitake Organic Mushrooms are recalled due to undeclared...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: BALL NOSE GUIDE WIRE 80CM Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Hip systems Recalled by Zimmer Biomet, Inc. Due to Elevated levels...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: HA Pins (DFS HA Cort Screw) Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive RS Cleat CAP Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Recalled by...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing