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.
Showing 2141–2160 of 51,038 recalls
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.
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.
Recalled Item: Infinia Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicam Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.