Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,040 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,040 in last 12 months

Showing 19341–19360 of 52,570 recalls

Medical DeviceApril 7, 2020· Maquet Cardiovascular, LLC

Recalled Item: Hemashield Gold Knitted Microvel Double Velour Vascular...

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· Inpeco S.A.

Recalled Item: FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...

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· 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-Thoracoabdominal...

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· Philips North America, LLC

Recalled Item: Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model:...

The Issue: If the shaft breaks due to material fatigue, the trauma arm can fall down...

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 using the Aliquoter Module (Inpeco P/N...

The Issue: In certain firmware versions, in case a Clot Detection error (error code...

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 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 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATION IMPACT 10CC and OSTEOVATION Recalled by Skeletal Kinetics, Llc...

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 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: 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: 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: OSTEOVATIONEX 5CC 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