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. 2,420 recalls have been distributed to Connecticut in the last 12 months.
Showing 35481–35500 of 51,038 recalls
Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...
The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...
The Issue: Dialyzer header leak due to possible improper torque
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...
The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...
The Issue: The firm has received one report of values for patient height and weight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telmisartan Tablets Recalled by Torrent Pharmaceuticals Limited Due to...
The Issue: Presence of Foreign Substance: Product complaint for the presence of foreign...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...
The Issue: The firm received a complaint of the battery exploding while recharging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...
The Issue: PureWick is recalling external catheter for women Wicks because the labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the Recalled by Ab...
The Issue: Wrong quantitative results may be displayed in a report from the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebound Air Walker Product Usage: Rebound Air Walkers are indicated Recalled...
The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unloader Custom Lite Product Usage: Unloader Custom Lite is an Recalled by...
The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.