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. 1,974 recalls have been distributed to Connecticut in the last 12 months.
Showing 12101–12120 of 28,245 recalls
Recalled Item: Contour VL Ureteral Stent Set 6FX22-30CM with .035 Sensor UPN: M006180156080...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .038 3CM FLEX STR/150CM Recalled by...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25. Recalled by Abbott Gmbh...
The Issue: An erroneous concentration value for hepatitis A virus was utilized during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom convenience kits containing Medline brand Sterile Pre-Saturated...
The Issue: Medline identified that there may be a potential for voids in the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN:...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX /150CM Recalled by...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN:...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor UPN: M006192132080...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17 Recalled...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15 Recalled...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart Pump Kit Recalled by Cardiac Assist, Inc Due to Failure to prime...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL3 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVE 2 Birthing Bed - Product Usage: is designated to Recalled by Linet...
The Issue: The UDI on the device label indicates incorrect manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemLung Kit - DL31 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus newborn care Olympic Brainz Monitor Recalled by Natus Neurology DBA...
The Issue: The OBM system functional test (impedance and noise) was not carried out on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRx4841A 1.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...
The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices s intended to be used Recalled...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.