Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1296112980 of 27,462 recalls

Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
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
Medical DeviceJuly 29, 2019· MOTEK MEDICAL B.V.

Recalled Item: Body Weight Support (BWS) Light Recalled by MOTEK MEDICAL B.V. Due to The...

The Issue: The firm discovered a potential manufacturing deviation of the yoke of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing