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. 2,408 recalls have been distributed to Connecticut in the last 12 months.
Showing 39061–39080 of 51,038 recalls
Recalled Item: Poco Dolce Bittersweet Chocolate: Aztec Chili Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poco Dolce Bittersweet Chocolate: Almond Coconut Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...
The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...
The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Base for Terumo Advanced Perfusion System 1 Recalled by Terumo...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint...
The Issue: Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...
The Issue: complaints of system malfunction and unintended, sudden movement at start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...
The Issue: Potential for uncured adhesive between the metal threaded insert and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azithromycin Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin 500 mg tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.