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. 2,636 recalls have been distributed to Connecticut in the last 12 months.
Showing 6181–6200 of 51,038 recalls
Recalled Item: Geissler's Supermarket Spicy Salmon 9.6 oz Ingredients read in part:...
The Issue: undeclared allergens (egg)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atovaquone Oral Suspension USP Recalled by AvKARE Due to Microbial...
The Issue: Microbial contamination of a non-sterile product: potential Bacillus cereus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isotretinoin Capsules Recalled by Teva Pharmaceuticals USA, Inc Due to...
The Issue: Superpotent Drug: The 3-month stability result for assay was found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HORIBA custom configured fluorescence instrument Recalled by Horiba...
The Issue: HORIBA custom configured fluorescence instrument has a laser safety defect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 13.0.0.1547 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 8.1.0.47 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9.0.0.113 and 9.0.1.142. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 11.0.0.951 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 8.0.0.61 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 15.0.0.430. Radiation Therapy Treatment Planning System. Recalled...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 7.0.0.19. Radiation Therapy Treatment Planning System. Recalled...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 10.0.0.1154 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 10.1.0.613 and 10.1.1.54. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 12.0.0.932 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System....
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9.1.0.933 and 9.2.0.483. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Femoral Component Recalled by Zimmer, Inc. Due to Out of...
The Issue: Out of specification violation of devices that results in a gap existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEXLIZET (bempedoic acid and ezetimibe) tablets Recalled by Esperion Due to...
The Issue: Failed dissolution specifications: out-of-specification bempedoic acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Newport s N-LHP-928(j) units if sold as a laser head/power supply set...
The Issue: According to 21 CFR 1040.10(f)(4), each laser system classified as a Class...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.