Product Recalls in District of Columbia

Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,616 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,616 in last 12 months

Showing 75217540 of 27,451 recalls

Medical DeviceAugust 24, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...

The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2022· SenTec AG

Recalled Item: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy Recalled by SenTec AG...

The Issue: Weak skin adhesion.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Magnesium (MG) Flex reagent cartridge Siemens Material Number...

The Issue: Dimension Magnesium (MG) Flex reagent cartridge lots may exhibit imprecision...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2022· Associates of Cape Cod, Inc.

Recalled Item: Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Recalled by...

The Issue: Incorrect information on the Fungitell STAT clamshells containing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide (Safe-T-J Curved) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Heavy Double Flexible Tipped Wire Guide Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Vinyl Connecting Tube Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Newton Wire Guide (LT Taper/10cm Distal Flexibility) Recalled by Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Bentson Plus Wire Guide (Extra Body/20cm Distal Flexibility with Softened...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Wire Guide (The Firm LT) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Rosen Curved Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Amplatz extra Stiff Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Double Flexible Tipped Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Cope Mandril Wire Guide (Stainless Steel) Recalled by Cook Incorporated Due...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Torq-Flex Wire Guide Australian Modification Recalled by Cook Incorporated...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing