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. 2,442 recalls have been distributed to Connecticut in the last 12 months.
Showing 32021–32040 of 51,038 recalls
Recalled Item: Biograph mCT X-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Donepezil Hydrochloride Tablets Recalled by Sandoz Inc Due to Subpotent...
The Issue: Subpotent Drug: out of specification results for assay test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nano PNC Water Recalled by Pacific Medical Solutions Due to Marketed without...
The Issue: Marketed without an Approved NDA/ANDA and non-sterility: NANO PNC Water by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Williams-Sonoma Meyer Lemon Poppy Quick bread mix Recalled by...
The Issue: Williams Sonoma was notified by their contract manufacturer that high heat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Source Naturals Dietary Supplement Vitamin D-3 Recalled by Threshold...
The Issue: Testing of Vitamin D-3 as a result of a consumer complaint found specific...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Extra-Virt Plus DHA Prenatal/Postnatal Softgel Recalled by VIRTUS...
The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VirtPrex Prenatal/Postnatal Tablets Recalled by VIRTUS PHARMACEUTICALS OPCO...
The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Virt-Advance Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS...
The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rabeprazole Sodium Delayed Release Tablets Recalled by Amneal...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Virt-Select Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS...
The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...
The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...
The Issue: Product was not sterilized. Product was shipped to distribution centers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...
The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...
The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...
The Issue: Olympus has received complaints regarding the breakage of the endoscope's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System Recalled...
The Issue: Merge received reports of Merge Eye Station being unable to capture images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bodega de San Antonio Sangria Traditional Basket #298 Recalled by Houdini...
The Issue: Potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.