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. 2,623 recalls have been distributed to Connecticut in the last 12 months.
Showing 7421–7440 of 28,245 recalls
Recalled Item: CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT Recalled...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm LifePort Endotracheal Tube Adapters 10-pack Recalled by Bunnell, Inc....
The Issue: Some adaptors, for use with high frequency ventilators, were packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product...
The Issue: Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used Recalled by NuVasive...
The Issue: During accelerated shelf-life extension studies it was noted that the final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in...
The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM...
The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak Surgical Procedure Pack Recalled by Alcon Research, LLC Due...
The Issue: Due to difficulty removing the liner on the adhesive components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0. Used to display medical images (Including...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0. Used to display...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE Recalled by...
The Issue: Upon review of its batch record, Southmedic identified that lot # W92761 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic...
The Issue: Confirmed an average positive bias of 40% for testosterone concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrackX Insight Base Modular Instrument Tracker Recalled by Trackx Technology...
The Issue: The device is breaking and falling off the Nuvasive T-Handle with Hudson...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.