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 54815500 of 47,654 recalls

Medical DeviceMay 14, 2024· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 Recalled by...

The Issue: The firm received reports that some blood collection tubes have experienced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate...

The Issue: Kit assigned an extended expiration date of 24-Jul-2025 during release. The...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2024· Applied Medical Technology Inc

Recalled Item: AMT Initial Placement Dilator Set. Used to place gastrostomy devices....

The Issue: Devices were labelled with the incorrect guidewire labelling.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2024· NxStage Medical Inc

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical Inc Due to The...

The Issue: The smaller chamber of the two chamber bag is bursting when nurses are...

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

Class II — Potential Health HazardOngoing
DrugMay 13, 2024· Golden State Medical Supply Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Golden State Medical Supply...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets Recalled by Glenmark...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets Recalled by Glenmark...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2024· American Regent, Inc.

Recalled Item: Vasopressin Injection Recalled by American Regent, Inc. Due to Subpotent...

The Issue: Subpotent product in addition to having out-of-specification results for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 13, 2024· SVS LLC

Recalled Item: Non-sterile Recalled by SVS LLC Due to Mislabeling

The Issue: Firm received complaints regarding skin irritation when using the gloves,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...

The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...

The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Aesculap Inc

Recalled Item: Aeos Robotic Digital Microscope Recalled by Aesculap Inc Due to Possibility...

The Issue: Possibility of the robotic arm to drop more than 10cm from its original...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· SIGHT DIAGNOSTICS LTD

Recalled Item: Sight OLO CBC Test Kit Recalled by SIGHT DIAGNOSTICS LTD Due to One Test Kit...

The Issue: One Test Kit lot (TK1-10114) shows a positive bias in the platelet count due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Draeger Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (IACS) Monitoring System Recalled by Draeger...

The Issue: Device is not in full compliance to Type CF requirements of IEC 60601-1 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in...

The Issue: The reason for recall is the meters may show an incorrect measurement unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Young Dental Manufacturing I, LLC

Recalled Item: Darby Prophylaxis Paste with 1.23% Fluoride Ion Recalled by Young Dental...

The Issue: Part number 040032, Lot number, 248607 was incorrectly labeled as part...

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

Class II — Potential Health HazardOngoing
FoodMay 10, 2024· Healthwest Minerals, Inc. dba Mt. Capra Products

Recalled Item: Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. Recalled by...

The Issue: The Goat Milk Formula Recipe Kit has been sold and marketed as infant...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Front label states 100 Tablets instead...

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

Class III — Low RiskOngoing
Refund