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. 2,408 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,408 in last 12 months

Showing 3694136960 of 51,038 recalls

FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Single Curry Chicken Salad Wrap Recalled by Whole Foods Market Group Inc....

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Classic Deli Pasta Salad Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Classic Deli Pasta Salad Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Curry Chicken Salad Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Classic Deli Pasta Salad Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: FP Pasta Salad Classic Deli Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: PPK Salad Chicken Curry Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Curry Chicken Salad CC Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Curry Chicken Salad Rollup Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2015· Whole Foods Market Group Inc.

Recalled Item: Curry Chicken Salad Wrap Recalled by Whole Foods Market Group Inc. Due to...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 22, 2015· Mercury Enterprises, Inc. dba Mercury Medical

Recalled Item: Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The...

The Issue: Incorrect use of T-Piece resuscitators will result in complete occlusion of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2015· Innokas Medical Oy

Recalled Item: CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans Recalled...

The Issue: Monitor may shut down unintentionally without restarting.

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2015· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: Presence of Foreign Tablets/Capsules: one foreign capsule identified as...

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

Class III — Low RiskOngoing
Refund
DrugOctober 21, 2015· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION Recalled by Vintage...

The Issue: Failed Stability Specifications: Out of Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Biopsy Starter Kit Recalled by Civco Medical Instruments Co. Inc. Due...

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 6F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 6F Recalled by...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 4F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 4F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing