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. 1,713 recalls have been distributed to District of Columbia in the last 12 months.
Showing 41721–41740 of 47,654 recalls
Recalled Item: Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71058-XX: 04.2mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: lM71059-XX: Indus Screw 04.2mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71016-XX: 04.5mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Snowball Cookies sold under the Lambs Farm brand and packaged Recalled by...
The Issue: The labels do not declare milk, soy, and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Banana Nut Bread loaf sold under the Lambs Farm brand Recalled by The Lambs...
The Issue: The labels do not declare soy allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blueberry Bread loaf sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare soy allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shortbread Almond Crescent cookies sold under the Lambs Farm brand Recalled...
The Issue: The labels do not declare milk, soy, and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raspberry Swirl Bread loaf sold under the Lambs Farm brand Recalled by The...
The Issue: The labels do not declare soy allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lemon Butter Cookies sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Double Chocolate Butter Cookies sold under the Lambs Farm brand Recalled by...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheerful Cookie Combo containing an assortment of Lemon Butter Cookies...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Famous Butter Cookies sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PCC Recalled by Nexgen Pharma, Inc. Due to Nexgen Pharma Inc. is recalling...
The Issue: Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest...
The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...
The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm...
The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.