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. 2,488 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,488 in last 12 months

Showing 2134121360 of 49,990 recalls

FoodJuly 30, 2019· Green Water, LLC

Recalled Item: Taspen s Organics Recalled by Green Water, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 30, 2019· Green Water, LLC

Recalled Item: Taspens Organics Recalled by Green Water, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 30, 2019· Green Water, LLC

Recalled Item: Taspens Organics Recalled by Green Water, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 30, 2019· Green Water, LLC

Recalled Item: Taspen s Organics Recalled by Green Water, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 30, 2019· Green Water, LLC

Recalled Item: Taspen s Organics Recalled by Green Water, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 30, 2019· Green Water, LLC

Recalled Item: Taspen s Organics Recalled by Green Water, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 30, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Digital Medical X-ray Imaging System Recalled by Shanghai United Imaging...

The Issue: X-ray imaging system positioning image and protocol label is reversed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Eizo Corporation

Recalled Item: RadiForce GX560 monochrome LCD monitor Recalled by Eizo Corporation Due to...

The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Eizo Corporation

Recalled Item: RadiForce RX360 Recalled by Eizo Corporation Due to Under certain...

The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000...

The Issue: Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan/CF: a) 3.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan/HVT: a) 5.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan Preformed: a) 3.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan Uncuffed: a) 2.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS: a) 4.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT Novaplus: a) 7.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to Reported...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System...

The Issue: Artis zee/Q systems patient tables may potentially have cracks in the table...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2019· Aurobindo Pharma USA Inc.

Recalled Item: Simvastatin Tablets Recalled by Aurobindo Pharma USA Inc. Due to Labeling;...

The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; some bottles labeled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund