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. 1,021 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16401–16420 of 47,654 recalls
Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...
The Issue: Shipping box may contain wrong model.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....
The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zerbaxa (ceftolozane and tazobactam) 1.5g per vial for injection Recalled by...
The Issue: Lack of assurance of sterility: The results of sterility tests of seven...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzhydrocodone and Acetaminophen Tablets Recalled by KVK-Tech, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...
The Issue: Misleading error messages and a gap in the Operator Manual which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnshLabs - SARS-CoV2 IgM ELISA (u-Capture) Recalled by Ansh Labs, LLC Due to...
The Issue: Labeling update; To reduce the risk of false positive/false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...
The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...
The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit (LCSU 4) Recalled by Laerdal Medical (Suzhou)...
The Issue: Component failures may cause the unit to lose all suction. Users will need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid...
The Issue: Bottles Missing Product Label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...
The Issue: Product may contain white particulates that are microbial in nature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...
The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...
The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A calculator/data processing module for clinical use is an electronic...
The Issue: A software error results in the unintentional removal of the serum-indices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROmorphone HCl 6 mg/30mL in 0.9% Sodium Chloride Injection (0.2 mg/mL)...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine sulfate 150 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Recalled by SCA Pharmaceuticals Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product confirmed to have yeast
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension 10mg Recalled by...
The Issue: Cross- contamination with other products: The excipient, Crospovidone, NF is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.