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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2286122880 of 27,462 recalls

Medical DeviceSeptember 4, 2014· Teleflex Medical

Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...

The Issue: Misbranding: Although the product labeling identifies the catheters as...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Luminos Agile Max system The Luminos Agile is intended Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2014· Arjo Hospital Equipment AB

Recalled Item: Pressure IQ Evolve Mattress Recalled by Arjo Hospital Equipment AB Due to...

The Issue: The firm received complaints regarding multiple mattresses were showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2014· Dako North America Inc.

Recalled Item: Dako Autostainer Link 48 with software version Dako Link 4.0.3 Recalled by...

The Issue: Dako is recalling the Dako Link 4.0.3 software on the Dako Autostainer Link...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2014· Merge Healthcare, Inc.

Recalled Item: eFilm Workstation 4.0 and 4.0.1. eFilm Workstation is one of Recalled by...

The Issue: There is an issue related to eFilm Workstation versions 4.0 and 4.0.1 when...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Mass CKMB Isoenzyme Calibrator (MMB CAL) an in Recalled by...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista® Mass...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2014· Mckesson Information Solutions LLC

Recalled Item: McKesson Cardiology" Hemo intended for complete physiological/hemodynamic...

The Issue: Software Error: The McKesson Cardiology Hemo calculation section incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: The Ysio Systems with software version VC10 The Ysio enables Recalled by...

The Issue: Siemens discovered that an unlikely error may occur on the Ysio system with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Charnley PN Retract & Handle Recalled by DePuy Orthopaedics, Inc. Due to The...

The Issue: The small extraction peg of the Charnley Pin Retractor and Handle set is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes Part number: 8900-4012...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Medical Patient Monitor is a Physiological Recalled by Spacelabs...

The Issue: The clinician did not realize the monitor was in END CASE mode and was...

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

Class II — Potential Health HazardOngoing