Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 997 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
997 in last 12 months

Showing 18781–18800 of 48,330 recalls

Medical DeviceApril 7, 2020· Inpeco S.A.

Recalled Item: Aptio 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· 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- 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· 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· 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· 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· Maquet Cardiovascular, LLC

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

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-Angled 4 Branch...

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: SKAFFOLD CMF IMPRESS (MP) 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: CRANIOSCULPT C 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 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 C 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 C 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: MEDTRONIC BONE VOID FILLER 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: CRANIOSCULPT 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: CRANIOSCULPT 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