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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 39281–39300 of 47,654 recalls
Recalled Item: Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling:...
The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyproheptadine HCl Syrup (Cyproheptadine HCl Oral Solution Recalled by...
The Issue: Failed Impurities/Degradation Specifications : Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of particulate matter: A returned customer sample was evaluated and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...
The Issue: Report received where the Align Radial Stem fractured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...
The Issue: The box of guides for a specific case arrived intact but contained two (2)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saba Shark Cartilage Complex Dietary Supplement Recalled by AMS Health...
The Issue: The product is being recalled due to the potential presence of Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hapi Pudding Recalled by J F C International Inc Due to Product's label...
The Issue: Product's label fails to declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Optima NM/CT 640 Recalled by GE Healthcare, LLC Due to GE is issuing this...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.