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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 47101–47120 of 47,654 recalls
Recalled Item: ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah Recalled by...
The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rejuvenate Modular Stems Stryker Ireland Carrigtwohill Industrial Estate...
The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Meter Recalled by Accutron Inc Due to Accutron is recalling the...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM Flowmeter Pkg H Recalled by Accutron Inc Due to Accutron is recalling the...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport Portable Package Recalled by Accutron Inc Due to Accutron is...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra PC% Cabinet Mount Package G Recalled by Accutron Inc Due to Accutron...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Motorola Solutions PCS3000/CS3070 Laser Utility/Peripheral Laser Products...
The Issue: It was discovered the CS3000/CS3070 was manufactured using the laser power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kimberly Clark Patient Warming System - Model 1000 Control Unit. Recalled by...
The Issue: A defect of the "fuse holder" can lead to a Control Unit failure that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma...
The Issue: Potential failure in the glued seal between the stem and the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipofilter 3000 Recalled by MicroAire Surgical Instruments, LLC Due to...
The Issue: Medical device was not manufactured under Good Manufacturing Procedures and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CABERGOLINE Tablets Recalled by Teva Pharmaceuticals USA, Inc. Due to...
The Issue: Impurities/Degradation Products: This lot of product will not meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine Injection Recalled by Luitpold Pharmaceuticals, Inc. Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The brand name of the device is Damon 3MX Bicuspid Bracket Recalled by...
The Issue: The firm initiated the recall as a result of a misidentification of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jolessa (levonorgestrel/ethinyl estradiol tablets Recalled by Teva...
The Issue: Contraceptive Tablets Out of Sequence: This recall has been initiated due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential issue due to image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplilink (AL) Software 3.2.3 for use with COBAS AMPLICOR Recalled by Roche...
The Issue: When using a Laboratory Information system (LIS) with automated systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMASpectrum Infusion Pump Master Drug Library (MDL) Editor software....
The Issue: Sigma is a safety alert for the Master Drug Library (MDL) Editor software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-ROCK For Men Recalled by XRock Industries, LLC Due to Marketed Without an...
The Issue: Marketed Without an Approved NDA/ANDA: product tested positive for PDE-5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Grafton DBM Matrix PLF Multiple Sizes Grafton is a human Recalled by...
The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...
The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.