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. 2,565 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,565 in last 12 months

Showing 1480114820 of 47,654 recalls

FoodJuly 26, 2021· CAHILLS FARM CHEESE LIMITED

Recalled Item: Lidl Preferred Selection-Irish Stout Cheddar - 7 oz. Recalled by CAHILLS...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2021· Monfefo LLC

Recalled Item: Monfefo brand Turmeric Shot Recalled by Monfefo LLC Due to Product was not...

The Issue: Product was not manufactured according to specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment SP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment NP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment WP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment MU Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment SU Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment PCA Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...

The Issue: Due to potential performance issues with software version 3.2.3 and earlier....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick Recalled by...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Cleansing Scrub Swabstick (1's) Recalled by Professional...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Prep Pad Large Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Swabstick (3's) Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Prep Pad MEDIUM Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodide Cleansing Scrub Swabstick (3's) Recalled by Professional...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidine Iodine Swabstick (1's) Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund