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. 1,058 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,058 in last 12 months

Showing 19601–19620 of 51,768 recalls

Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Inpeco S.A.

Recalled Item: Abbott Accelerator a3600 Recalled by Inpeco S.A. Due to When analyzer sample...

The Issue: When analyzer sample carousel lid remains open or manual process is too...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Inpeco S.A.

Recalled Item: Inpeco FlexLab Recalled by Inpeco S.A. Due to When analyzer sample carousel...

The Issue: When analyzer sample carousel lid remains open or manual process is too...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch Recalled by...

The Issue: Potential small holes at the seam lines of Hemashield branches causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Inpeco S.A.

Recalled Item: Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N...

The Issue: The identified problem is an erroneous association between the carrier and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2020· Innovasis, Inc

Recalled Item: Oryx Cervical Screw Caddy Recalled by Innovasis, Inc Due to Cervical screw...

The Issue: Cervical screw caddies have incorrect text markings for the 4.5mm Fixed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: EXACTECH OSSILIX FORM (MX) Recalled by Skeletal Kinetics, Llc Due to Bone...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATIONEX 2CC INJECT FORMULA. Product Number: 390-0002 Recalled by...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: ACUMED IMPACT 5CC. Product Number: 65-0105-S Recalled by Skeletal Kinetics,...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: EXACTECH OSSILIX MP FIL Recalled by Skeletal Kinetics, Llc Due to Bone void...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: ACUMED CALLOS INJECT 3CC. Product Number: 65-0003-S Recalled by Skeletal...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: ACUMED IMPACT 10CC. Product Number: 65-0110-S Recalled by Skeletal Kinetics,...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATION EX Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: EXACTECH OSSILIX FORM (MX) Recalled by Skeletal Kinetics, Llc Due to Bone...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATION Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: SKAFFOLD RENU FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing