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. 2,664 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,664 in last 12 months

Showing 18811900 of 51,038 recalls

Medical DeviceJuly 17, 2025· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control...

The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...

The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· Quest International, Inc.

Recalled Item: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant...

The Issue: Measles IgM Test Kit lacks premarket approval or clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· O&M HALYARD INC

Recalled Item: Orthopedic Pack Recalled by O&M HALYARD INC Due to Surgical drape packs may...

The Issue: Surgical drape packs may have open seals, which may compromise the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· Medtronic Xomed, Inc.

Recalled Item: IPC Powerease System UDI-DI: 00613994448705 00643169406834. The IPC Recalled...

The Issue: Due to out of the box wobble of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· Philips Medical Systems (Cleveland) Inc

Recalled Item: Pinnacle 3 with TumorLOC Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: Due to software issue, Radiation Therapy Planning system may provide...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2025· QUEEN BEE GARDENS

Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Intended use:...

The Issue: Product may have small flakes of stainless steel in product.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2025· QUEEN BEE GARDENS

Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: Recalled by...

The Issue: Product may have small flakes of stainless steel in product.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2025· QUEEN BEE GARDENS

Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Intended use:...

The Issue: Product may have small flakes of stainless steel in product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 16, 2025· PREMIA SPINE LTD

Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...

The Issue: Potential for missing pins at tip of inserter.

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

Class II — Potential Health HazardOngoing
DrugJuly 15, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 15, 2025· Stryker Communications

Recalled Item: Chromophare Surgical Light System Recalled by Stryker Communications Due to...

The Issue: Surgical lights have stress lines forming on the powder coating, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Prosthesis Head B Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Inconsistent size terminology and color coding used on labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Plastic Trial Head Brown Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: Inconsistent size terminology and color coding used on labeling

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

Class II — Potential Health HazardOngoing
FoodJuly 14, 2025· NuNaturals Inc

Recalled Item: Pure Monk Fruit Sweetener Recalled by NuNaturals Inc Due to Product is...

The Issue: Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 14, 2025· NuNaturals Inc

Recalled Item: Organic Pure Stevia Recalled by NuNaturals Inc Due to Product is Monk Fruit...

The Issue: Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 14, 2025· World Market Management Services, LLC

Recalled Item: Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. Recalled by...

The Issue: Salmonella. The firm was notified by the FDA that the product may be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 14, 2025· MAQUET GMBH

Recalled Item: Corin Operating Tables Model Numbers: (1) 770001A0 Recalled by MAQUET GMBH...

The Issue: Under certain conditions, such as the simultaneous use of the operating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic...

The Issue: Specific lots of reprocessed electrophysiology catheters may contain small...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 14, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Novum IQ Large Volume Pump Recalled by Baxter Healthcare Corporation...

The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large...

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

Class I — Serious Health HazardOngoing