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. 2,092 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,092 in last 12 months

Showing 21412160 of 51,038 recalls

DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg Recalled by Lupin...

The Issue: Product Mix Up: This product is being recalled because of a complaint...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2025· Intersurgical Inc

Recalled Item: One-piece Guedel airway Recalled by Intersurgical Inc Due to Potential...

The Issue: Potential contamination with small burrs, which if detach could be inhaled...

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2025· CinFranky LLC dba New Mexico Pinon Coffee

Recalled Item: New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Recalled by...

The Issue: Clear coat seal on the lid of the single serve cups did not get applied...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...

The Issue: Defective container; blister packaging inadequately sealed.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...

The Issue: Defective container; blister packaging inadequately sealed.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 18, 2025· C.R. Bard Inc

Recalled Item: Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated...

The Issue: Foley catheter may have an obstructed lumen, which may result in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Osteotec Limited

Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...

The Issue: There is the potential that the silicone implant may contain foreign material

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Medtronic, Inc.

Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....

The Issue: In prior SmartSync application versions, the Abort button stopped the test...

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

Class II — Potential Health HazardOngoing
FoodJune 18, 2025· Lipari Foods Operating Company, LLC.

Recalled Item: JLM Manufacturing Dark Chocolate Nonpareils Recalled by Lipari Foods...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 18, 2025· Prestige Brands Holdings

Recalled Item: Little Remedies¿ Honey Cough 4 FL OZ (118 mL) Recalled by Prestige Brands...

The Issue: contaminated with Bacillus cereus and may be spoiled

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule....

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable...

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable...

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 18, 2025· Medtronic, Inc.

Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...

The Issue: In prior SmartSync application versions, the Abort button stopped the test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· CARIS LIFE SCIENCES

Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...

The Issue: Due to an incorrect test results provided that indicated the incorrect drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· Quidel Corporation

Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...

The Issue: Dipstick strep A test has potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 90 Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing