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. 2,612 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,612 in last 12 months

Showing 94619480 of 47,654 recalls

DrugMarch 13, 2023· Direct Rx

Recalled Item: Ropinirole Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Glimepiride Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Glimepiride Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Ropinirole Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Simvastatin Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Finasteride Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Montelukast Sodium Tablets Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2023· Direct Rx

Recalled Item: Simvastatin Recalled by Direct Rx Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 13, 2023· TIPPCON LLC

Recalled Item: Perrona Hot Sauce Original with Chiltepin Peppers 5 fl oz Recalled by...

The Issue: Mold growth on the outside of the bottle

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

Class III — Low RiskOngoing
Refund
FoodMarch 13, 2023· TIPPCON LLC

Recalled Item: Perrona Hot Sauce Black with Chiltepin Peppers Net 5 FL Recalled by TIPPCON...

The Issue: Mold growth on the outside of the bottle

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

Class III — Low RiskOngoing
Refund
FoodMarch 13, 2023· TIPPCON LLC

Recalled Item: Perrona Hot Sauce Green with Chiltepin Peppers Net 5 FL Recalled by TIPPCON...

The Issue: Mold growth on the outside of the bottle

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 13, 2023· Spectrum Medical Ltd.

Recalled Item: Quantum Perfusion Systems for CPB Recalled by Spectrum Medical Ltd. Due to...

The Issue: The ratchet and pawl had an out of tolerance geometry which exhibited as the...

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

Class II — Potential Health HazardOngoing
DrugMarch 10, 2023· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2023· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2023· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2023· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System- For use in the in vitro quantitative Recalled...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing