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. 1,839 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,839 in last 12 months

Showing 3372133740 of 51,038 recalls

FoodJuly 11, 2016· HVL, LLC

Recalled Item: METABOLIC CLEANSE REVISED 1181 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: METABOLIC CLEASNSE VEG 1151 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· C.R. Bard, Inc.

Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to The product contained a...

The Issue: The product contained a latex catheter instead of a silicone catheter.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Operating Table TruSystem 7000 U Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Mobile Column TruSystem 7500 Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Floor Mounting Column TS 7500 U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Stationary Column TruSystem 7599 Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
FoodJuly 8, 2016· Montana Flour & Grains, Inc

Recalled Item: 100% Organic Spelt Grain Recalled by Montana Flour & Grains, Inc Due to...

The Issue: Organic Spelt Grain is recalled because label does not declare wheat.

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

Class II — Potential Health HazardOngoing
Refund