Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,495 recalls have been distributed to Delaware in the last 12 months.
Showing 19721–19740 of 27,373 recalls
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: 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: 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: 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: 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: 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. 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 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: 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: 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: 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: 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 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: Rebound Diabetic Walker Product Usage: Rebound Diabetic Walkers are used...
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: Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an...
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: Knee Undersleeve Gray Product Usage: Knee undersleeves are worn as 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: Rebound Cartilage Product Usage: Rebound Cartilage is an external knee...
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.
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: 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.