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. 2,420 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,420 in last 12 months

Showing 3638136400 of 51,038 recalls

Medical DeviceDecember 9, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2015· Philips Ultrasound, Inc.

Recalled Item: Philips Lumify Diagnostic Ultrasound Recalled by Philips Ultrasound, Inc....

The Issue: Color Flow direction is displayed incorrectly in Lumify 1.0. The system...

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

Class II — Potential Health HazardOngoing
DrugDecember 9, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Pink Bikini capsules Recalled by Lucy's Weight Loss (dba. Waisted With Lucy)...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 9, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Shorts on the Beach capsules Recalled by Lucy's Weight Loss (dba. Waisted...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synvasive Technology Inc

Recalled Item: Zimmer Oscillating Flat - TS ST Hub Recalled by Synvasive Technology Inc Due...

The Issue: Two lots of oscillating saw blades incorrectly identify the blade cutting...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
FoodDecember 8, 2015· Nuovo Pasta Productions, Ltd

Recalled Item: Simply Enjoy Shrimp and Lobster Ravioli Recalled by Nuovo Pasta Productions,...

The Issue: Shrimp and Lobster Ravioli back panel incorrectly identifies Spinach and...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: Morrison's Cornbread Mix NET WT 5 LB (2.27 kg) Recalled by C. H. Guenther &...

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: HEB Original Seasonal Catfish Fry Mix NET WT. 10 OZ Recalled by C. H....

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund