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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,639 in last 12 months

Showing 41814200 of 47,654 recalls

DrugSeptember 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...

The Issue: cGMP violations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: EPINEPHrine 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi...

The Issue: cGMP violations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Oxytocin 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi...

The Issue: cGMP violations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...

The Issue: cGMP violations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...

The Issue: CGMP violations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...

The Issue: cGMP violations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2024· Cardinal Health 200, LLC

Recalled Item: Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack...

The Issue: Certain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 25, 2024· Biocare Medical, LLC

Recalled Item: intelliPATH Universal HRP Detection Kit Recalled by Biocare Medical, LLC Due...

The Issue: Kits containing the DAB chromogen buffer, intended for use in either manual...

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

Class II — Potential Health HazardOngoing
FoodSeptember 24, 2024· Tropical Nut & Fruit Company

Recalled Item: Grabeez The Big Cheese SNACK MIX Net Wt. 3.25 oz Recalled by Tropical Nut &...

The Issue: Undeclared Almonds & Cashews. The firm was notified by their customers that...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2024· Nivagen Pharmaceuticals Inc

Recalled Item: Atorvastatin Calcium Tablets Recalled by Nivagen Pharmaceuticals Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray...

The Issue: Defective Delivery System: The dip tube is clogged causing the spray not to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2024· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System Recalled...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2024· Onkos Surgical, Inc.

Recalled Item: ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of...

The Issue: Potential challenge with intraoperative assembly of the external taper of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard PACEMAKER PACK - Medical convenience kits Model Number: MAMC223-08...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard D & C PACK-CKC - Medical convenience kits Model Number: BMGT003-02...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing