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. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34541–34560 of 47,654 recalls
Recalled Item: Colostrum Powder Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PerCoBa Whey Protein Isolate with Colostrum Recalled by Immuno - Dynamics,...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: My Spice Sage Ground Flax Seed Meal under the following Recalled by Zenobia...
The Issue: Zenobia Company, LLC is recalling Flax Seed Meal due to the possible...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baclofen USP powder Recalled by Freedom Pharmaceuticals Inc Due to Presence...
The Issue: Presence of Foreign Substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...
The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...
The Issue: The product may contain electronic components that lead to a premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...
The Issue: Testing at customer site showed unit Remote Patient Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unolok Blunt Fill Needle 18G x 1.5" Red Recalled by Myco Medical Supplies...
The Issue: Particulates: Complaints of rubber coring from the closure of injection vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10) Recalled...
The Issue: Antibiotic concentration may be insufficient which may result in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Destination Renal Guiding Sheath Intended for the introduction of...
The Issue: Based on internal investigation and testing that revealed the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements are applications for radiation treatment planning for use...
The Issue: Large objects with fine resolution are potentially displayed cropped when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements are applications for radiation treatment planning for use...
The Issue: Large objects with fine resolution are potentially displayed cropped when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump SmartSite Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...
The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.