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. 961 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
961 in last 12 months

Showing 25321–25340 of 47,654 recalls

FoodMay 2, 2018· Utz Quality Food Inc

Recalled Item: Weis Signature Collection No Salt Added White Corn Tortilla Chips Recalled...

The Issue: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2018· Utz Quality Food Inc

Recalled Item: Utz Organic Yellow Corn Tortillas Recalled by Utz Quality Food Inc Due to...

The Issue: Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 1, 2018· AuroMedics Pharma LLC

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by AuroMedics Pharma LLC...

The Issue: Presence of Particulate Matter: confirmed customer report for presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 1, 2018· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2018· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2018· AuroMedics Pharma LLC

Recalled Item: Ampicillin and Sulbactam for Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Presence of Particulate Matter: confirmed customer report of the presence of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Hobbs Medical, Inc.

Recalled Item: Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to...

The Issue: Device was marketed for uses outside the 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zeego Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing