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. 1,074 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,074 in last 12 months

Showing 16221–16240 of 51,038 recalls

Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: ComfortGel - assists in the prevention and treatment of all Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Exactech, Inc.

Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....

The Issue: The HAT trial contains a retaining ring that has shown the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Skytron, Div. The KMW Group, Inc

Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...

The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: DiBAR LABS Hand Sanitizer (ethyl alcohol 70%) Recalled by DIBAR NUTRICIONAL...

The Issue: Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 11, 2021· DASH XCLUSIVE

Recalled Item: Imperia Elita Vitaccino Coffee Recalled by DASH XCLUSIVE Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis determined presence of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: DiBAR LABS Hand Sanitizer Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: ADVANCE HAND SANITIZER Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: ProtectoRx (ethyl alcohol 70%) Recalled by DIBAR NUTRICIONAL S DE RL DE CV...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2021· Ventec Life Systems, Inc.

Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...

The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· BioFire Diagnostics, LLC

Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...

The Issue: Elevated rates of false negative results may occur when using blood culture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Randox Laboratories Ltd.

Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...

The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· IMPLANTCAST GMBH

Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...

The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2021· K2M, Inc

Recalled Item: Cascadia AN Interbody Convex 10x22x15mm Catalog Number: 6101-2102215NC-G2...

The Issue: Mislabeled product labeling incorrect length or height, or length and height...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer...

The Issue: Fifty (50) individual units from Lot D20111130 were distributed with the...

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

Class II — Potential Health HazardOngoing