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. 2,567 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14421–14440 of 47,654 recalls
Recalled Item: Zonisamide Capsules USP 100 mg Rx Only Manufactured by: Glenmark Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF Recalled by DuPont...
The Issue: Microbial Contamination of Non-Sterile Product: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arformoterol Tartrate Inhalation Solution 15 mcg*/2 mL For Oral Inhalation...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...
The Issue: When a measurement with a PTW detector array is performed with the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part...
The Issue: Due to product not meeting specification for concentricity and failing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoLotion Transmission Lotion Recalled by North Coast Medical Inc Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by AVRIO...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...
The Issue: The product package may potentially contain a mismatched graft that does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rompe Pecho Max Multi-Symptoms Maximum Strength Recalled by Efficient...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rompe Pecho Ex Expectorant Recalled by Efficient Laboratories, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.