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. 2,415 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,415 in last 12 months

Showing 2042120440 of 27,462 recalls

Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...

The Issue: The door latch may not fully close and the door may open unexpectedly. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 11, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 10, 2015· Iba Dosimetry Gmbh

Recalled Item: IBA Dosimetry GmbH Lift Table Type 4320 Recalled by Iba Dosimetry Gmbh Due...

The Issue: When the electric lift table is connected to the mains power, in a very rare...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Flow-i Anesthesia System Product Usage: The indication for the Flow-i...

The Issue: Electrical issues in the control, monitoring or panel sub-systems, caused by...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Possible installation error of the quench lines of superconducting magnets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2015· Steris Corporation

Recalled Item: Quick Connects. Steris Corporation. Model numbers: QKC1736E Recalled by...

The Issue: The firm discovered that one of the hysteroscope models listed for...

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

Class II — Potential Health HazardOngoing