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. 2,426 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,426 in last 12 months

Showing 3380133820 of 51,038 recalls

FoodJuly 6, 2016· Kabobs Inc

Recalled Item: MINI FLORENTINE QUICHE Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: VEGETABLE SPRINGROLL Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: COZY SHRIMP Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: WILD MUSHROOM IN PHYLLO Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: MINI VEGETABLE EGGROLL Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: MUSHROOM TART Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: VEGETABLE EMPANADA Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: SWEET POTATO PUFF Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: COCONUT SHRIMP Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2016· Newly Weds Foods Inc

Recalled Item: Bulk flour bland breader packaged into 15 Recalled by Newly Weds Foods Inc...

The Issue: Flour contaminated with E. coli O121 was used in the manufacuring of flour...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2016· Branan Medical Corporation

Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...

The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...

The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...

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

Class III — Low RiskOngoing
DrugJuly 5, 2016· Let's Talk Health, Inc.

Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...

The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing