Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2688126900 of 28,127 recalls

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 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 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· 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 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· 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· 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: 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 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 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
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· The Binding Site Group, Ltd.

Recalled Item: Digital RID Plate Reader and Software Product Code: AD400 Recalled by The...

The Issue: If a control ring is marked after reading, the software will not flag...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method...

The Issue: Siemens Healthcare Diagnostics has confirmed the potential for falsely...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2012· Radiometer America Inc

Recalled Item: Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The...

The Issue: RADIOMETER became aware that some membranes may have enzyme residue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2012· Philips Medical Systems (Cleveland), Inc.

Recalled Item: Pinnacle3 VCC P/N 4598 001 41341 REV A Recalled by Philips Medical Systems...

The Issue: Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2012· Spacelabs Healthcare, Llc

Recalled Item: The touchscreen display (model 94267) designed for use with the Recalled by...

The Issue: Potential failure of Spacelabs Healthcare Touchscreen Display, Model 94267...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2012· Biomet, Inc.

Recalled Item: Ranawat/Burnstein Acetabular Shell 54mm/Limited Holes/Porous Coated is a...

The Issue: The color code on label conflicts with the liner size (liner size 24 should...

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

Class II — Potential Health HazardOngoing