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. 1,054 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,054 in last 12 months

Showing 17521–17540 of 51,038 recalls

Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2020· VISBY MEDICAL INC

Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...

The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...

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

Class II — Potential Health HazardOngoing
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Zydus...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2020· Medela AG Medical Technology

Recalled Item: Stryker Medela .0193 AXS Universal Aspiration Tubing (01)07612367053921 -...

The Issue: Incorrect expiration date of "2023-07-24" on label of sterile tubing....

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2020· Flowers Foods (Corporate Offices)

Recalled Item: CANYON BAKEHOUSE GLUTEN MOUNTAIN WHITE BREAD NET WT. 18oz (1lb Recalled by...

The Issue: The firm discovered that some of their products showed higher than...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2020· Flowers Foods (Corporate Offices)

Recalled Item: CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ Recalled by...

The Issue: The firm discovered that some of their products showed higher than...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Prof (Professional) Meters- IVD professional healthcare...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS PST Meters- IVD (Patient Self-Testing) measures blood-clotting...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 154 cm (61 IN) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 9"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box Recalled...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18cm) APPX 0.43ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing