Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,724 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,724 in last 12 months

Showing 1814118160 of 51,768 recalls

Medical DeviceSeptember 14, 2020· Invivo Corporation

Recalled Item: MR Coils The MR Coil is intended to be used Recalled by Invivo Corporation...

The Issue: The labels have been mistakenly printed with an IPX1 rating symbol. IPX...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650301023 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650301018 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #65021652 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650600111 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #65220955 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650304917 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650305414 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #65193091 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and...

The Issue: The device may detect an incorrect Heater Bag volume which may lead to a...

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

Class II — Potential Health HazardOngoing
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Panagel Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse PACS Software Versions 5.1 and higher Recalled by Fujifilm Medical...

The Issue: There is a potential for the wrong patient information may be displayed in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Bien-Air Surgery SN ******* MULTIFUNCTION PEDAL OSSEODUO - Recalled by...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Bien-Air Surgery SN ******* OSSEOSTAP Footcontrol - Product Recalled by...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse PACS Software Version 5.6.1 - Product Usage: intended for Recalled...

The Issue: FUJIFILM has become aware of the possibility that certain CT studies may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Bien-Air Surgery SN **** FOOTCTRL OSSEODOC - Product Recalled by Bien-Air...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing