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 2596125980 of 28,127 recalls

Medical DeviceApril 30, 2013· Elekta, Inc.

Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...

The Issue: Unexpected movement during beam delivery may not be detected if there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2013· Biomet, Inc.

Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...

The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Beckman Coulter Inc.

Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...

The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Cardio Medical Products

Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...

The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Instratek, Incorporated

Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...

The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******microMax Handpiece***Rx Only***Manufacturer: The Anspach Effort...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...

The Issue: Philips has received one report from the field that there was an unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...

The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...

The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2013· Embla System Llc

Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...

The Issue: Calibration error for Embla Embletta Gold units calibrated through service...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing