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. 2,456 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,456 in last 12 months

Showing 2534125360 of 51,038 recalls

DrugAugust 8, 2018· Hetero Labs Limited Unit V

Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2018· Philips North America LLC

Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...

The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...

The Issue: Two units in distribution were found to be mislabeled on the vial cap with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Helena Laboratories, Corp.

Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...

The Issue: The positive control on some tests of the lots did not appropriately react...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Helena Laboratories, Corp.

Recalled Item: ColoCARE Recalled by Helena Laboratories, Corp. Due to The positive control...

The Issue: The positive control on some tests of the lots did not appropriately react...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect simply RePlant Implant Recalled by Implant Direct Sybron...

The Issue: The incorrect device was packaged in the vial.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
DrugAugust 7, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Doxycycline Hyclate USP Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp....

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2018· Natures Bounty Inc

Recalled Item: BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH...

The Issue: High level of microcystin observed in the product.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2018· Country Favor Inc.

Recalled Item: BEST TASTE BRAND SNACK GINGER SLICED Recalled by Country Favor Inc. Due to...

The Issue: Product contains high levels of undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 6, 2018· Dannoritzer Medizintechnik GmbH & Co. KG

Recalled Item: Laparoscopy Instruments Instructions For Use (IFU) for the following:...

The Issue: The Manual cleaning process and the usability of the reprocessing...

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

Class III — Low RiskOngoing
Medical DeviceAugust 3, 2018· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to Order...

The Issue: Order Status Remains Approved When Should Indicate Complete.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...

The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...

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

Class II — Potential Health HazardOngoing
FoodAugust 3, 2018· Hostess Brands, LLC

Recalled Item: Hostess Brownies Cookies 'n Cr¿me packaged in the following ways: Recalled...

The Issue: The product ingredients statement declares egg ingredients, but the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2018· J R Simplot Co Corporate HQ

Recalled Item: Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend Recalled by...

The Issue: Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend is recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: Best Choice Recalled by Product Quest Manufacturing LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: Harmon Face Values Recalled by Product Quest Manufacturing LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund