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. 2,461 recalls have been distributed to Connecticut in the last 12 months.
Showing 23621–23640 of 51,038 recalls
Recalled Item: Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyhexamethylene Biguanide 0.02% Ophthalmic Drops Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine 1 mg/mL Injection Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 20 Day Extra Strength Recalled by Anderson Compounding Pharmacy, Inc....
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Quad-Mix 20:30:1:0.15 Injection Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenol 10% Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Tri-Mix 50:30:1 Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...
The Issue: Pin hole package failures compromising sterility of product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Incorrect part description contained on an additional label placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...
The Issue: There is a potential for the single use suction valve to come apart and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope Recalled by Verathon, Inc. Due to A...
The Issue: A typographical error in the Operations & Maintenance Manual incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...
The Issue: Stability did not meet acceptance criteria for visual appearance during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breads from Anna Classic Herb Bread Mix 19oz Recalled by Wholesome Treats,...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breads from Anna Black Bean Brownie Mix 14oz Recalled by Wholesome Treats,...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.