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. 1,975 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,975 in last 12 months

Showing 78417860 of 28,245 recalls

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 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· 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· 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+ 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 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+ 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
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 23, 2022· Family Dollar Stores, Llc.

Recalled Item: DENTEMP ONE STEP .077OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ Recalled by Family Dollar Stores,...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT Recalled by Family Dollar Stores,...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ Recalled by Family Dollar Stores, Llc....

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: KY JELLY LUBRICANT 2 FL OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: SIMPLY SALINE NASAL MIST 3.1 OZ Recalled by Family Dollar Stores, Llc. Due...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Affected...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

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

Recalled Item: Veriquick Pregnancy Test 2CT Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· DICOM Grid, Inc. d/b/a Ambra Health

Recalled Item: Ambra PACS Recalled by DICOM Grid, Inc. d/b/a Ambra Health Due to A race...

The Issue: A race condition between the storage system and services database has the...

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

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

Recalled Item: CURAD STRNG WATRPRF STRIP 1IN 20CT Recalled by Family Dollar Stores, Llc....

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing