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. 2,629 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,629 in last 12 months

Showing 62616280 of 47,654 recalls

Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Yueh Centesis Disposable Catheter Needle - Intended for use in Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Chiba Biopsy Needle - Used for aspiration biopsy. PART Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Floaters Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Allergy Eyes Relief Recalled by Optikem International, Inc....

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Pink Eye Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Aging Eye Relief Recalled by Optikem International, Inc....

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Eye strain Relief Recalled by Optikem International, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Red Eye Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Eye Twitching Relief Recalled by Optikem International, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund