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. 2,457 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,457 in last 12 months

Showing 2614126160 of 27,373 recalls

Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Invivo Corporation

Recalled Item: Invivo Corporation Expression MRI Patient Monitoring System. The Expression...

The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Toshiba American Medical Systems Inc

Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...

The Issue: It was found that there is a problem with the LCD monitor used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Ossur Americas, Inc.

Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...

The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· GE Healthcare, LLC

Recalled Item: GE Discovery NM/CT670 Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: Recalled by...

The Issue: There is a small risk of a leak in Cycler Sets and if the Cycler Set is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· MOOG Medical Devices Group

Recalled Item: Infinity Enteralite Ambulatory Feeding Pumps Recalled by MOOG Medical...

The Issue: The firm is adding an addendum to the operator's manual for Infinity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: The Stryker Model 6390 Recalled by Stryker Medical Division of Stryker...

The Issue: Model 6390 Power-LOAD systems built between September 12, 2012 and September...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...

The Issue: Firm has received reports from customers that the small pins at the bottom...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: PENTRA C200 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA AST CP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilette Mira Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There is a risk of lost images during examination.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL...

The Issue: Correlation slope bias and accuracy shift

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 10, 2012· Alfa Wassermann, Inc.

Recalled Item: Alfa Wassermann System Diluent 750 mL Manufactured for Alfa Wassermann...

The Issue: Inorganic phosphorus assays using System Diluent Lot 155599 may not product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: MAVIG PORTEGRA 2 system operated in conjuction with a Siemens Recalled by...

The Issue: A particular component may not have been fitted during the installation of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...

The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...

The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin...

The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing