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. 2,590 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,590 in last 12 months

Showing 1226112280 of 51,038 recalls

DrugJune 24, 2022· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Customer complaints received for ripping patches...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2022· Neotract Inc

Recalled Item: UroLift System Recalled by Neotract Inc Due to There is the potential that...

The Issue: There is the potential that during implant deployment, the device may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Medtronic Inc

Recalled Item: Medline Sprinter OTW Recalled by Medtronic Inc Due to Luer has balloon...

The Issue: Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Stryker Instruments

Recalled Item: Stryker 2.3mm Tapered Router Recalled by Stryker Instruments Due to There is...

The Issue: There is a potential for the core diameter to be undersized, which may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Zeiss, Carl Inc

Recalled Item: ZEISS Axio Observer 5 microscope Recalled by Zeiss, Carl Inc Due to An...

The Issue: An incorrect Unique Device Identification (UDI) label was installed on some...

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

Class III — Low RiskOngoing
Medical DeviceJune 24, 2022· GE Healthcare, LLC

Recalled Item: SIGNA Premier magnetic resonance scanner Recalled by GE Healthcare, LLC Due...

The Issue: Under rare conditions, SIGNA Premier gradient coils could result in elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress Recalled by Baxter...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress Recalled by...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Centrella Pro+ 40" Surface mattress Recalled by Baxter Healthcare...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Centrella Pro+ 36" Surface mattress Recalled by Baxter Healthcare...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress Recalled by Baxter...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare mattress Recalled by Baxter...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ 36" MRS Surface mattress Recalled by Baxter Healthcare...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: QP COUGH COLD TABLET 16 CT distributed to specific Family Recalled by Family...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: NPX ENEMA 4.5 FL OZ 2 PK distributed to specific Recalled by Family Dollar...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: MIDOL COMPLETE CAPLET 16 CT SKU 913028 QP MENSTRUAL RELIEF Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: AMBI NRSHNG DAILY FACIAL MSTURZER 1.7 OZ distributed to specific Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: DR SCHOLLS CLR AWAY LIQ WART REMVR 20CT SKU 998384 Recalled by Family Dollar...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: GUARDIAN ANTACID EX STRGTH TBLT FRT 96CT SKU 901379 GUARDIAN Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund