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. 2,628 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,628 in last 12 months

Showing 63816400 of 51,038 recalls

Medical DeviceMarch 11, 2024· Conformis, Inc.

Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...

The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...

The Issue: Black particulate matter from the carbon filter component of the canisters...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...

The Issue: Black particulate matter from the carbon filter component of the canisters...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Baxter Healthcare Corporation

Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2024· Noah Medical

Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...

The Issue: Due to a misaligned calibration of the wired controller that may result in...

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

Class II — Potential Health HazardOngoing
FoodMarch 7, 2024· RAJA FOODS LLC

Recalled Item: SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags Recalled by RAJA...

The Issue: Product tested positive for lead

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 7, 2024· John B. Sanfilippo & Son Inc.

Recalled Item: Great Value Honey Roasted Cashews Recalled by John B. Sanfilippo & Son Inc....

The Issue: undeclared milk and coconut

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 7, 2024· Stonewall Kitchen, LLC

Recalled Item: Stonewall Kitchen Cinnamon Sugar Doughnut Mix Recalled by Stonewall Kitchen,...

The Issue: Product contains undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Tri-Lo-Sprintec (norgestimate and ethinyl estradiol) tablets USP - triphasic...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
FoodMarch 6, 2024· Colonna Brothers Inc.

Recalled Item: Supreme Tradition brand and Marcum brand ground cinnamon. Packaged in...

The Issue: Elevated lead levels in cinnamon

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2024· B. Braun Medical Inc

Recalled Item: Potassium Chloride for Injection Concentrate USP Recalled by B. Braun...

The Issue: Lack of assurance of sterility: pinholes, within the blue label characters...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2024· Artivion, Inc

Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...

The Issue: The blood cultures performed as part of the organ donation process were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Microbiologics Inc

Recalled Item: KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b Recalled by...

The Issue: The positive control material (Rhizopus stolonifer) within the KWIK-STIK...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe Constrained Humeral Liner: Item Numbers: a) 320-40-10...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing