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 41501–41520 of 47,654 recalls
Recalled Item: Bueno GC NM Hot 28oz Recalled by El Encanto, Incorporated Due to Potential...
The Issue: Products were recalled due to possible Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bueno GC NM Hatch Valley Hot 5-5# Z Recalled by El Encanto, Incorporated Due...
The Issue: Products were recalled due to possible Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bueno GC NM Mild 5-5# Z Recalled by El Encanto, Incorporated Due to...
The Issue: Products were recalled due to possible Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bueno GC NM Hatch Valley Mild 2-12.5# Z Recalled by El Encanto, Incorporated...
The Issue: Products were recalled due to possible Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Gaymar Medi-Therm device provides a means of regulating patient Recalled...
The Issue: Stryker Medical has identified that on some units of the MTA7900, there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health,...
The Issue: Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...
The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter- Confimed customer complaint of particulates...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carisoprodol Tablets Recalled by Watson Laboratories Inc Due to Presence of...
The Issue: Presence of Foreign Substance; metal particulates were visually observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...
The Issue: Images may be archived to an incorrect or invalid archive location resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...
The Issue: The locking mechanism that is intended to hold the control panel in a fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...
The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15%...
The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9%...
The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...
The Issue: Failed Tablet/Capsule Specifications: Split tablets were found in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...
The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...
The Issue: There is a potential for communication loss associated with the F5-01 Frame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.