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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 19021–19040 of 47,654 recalls
Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...
The Issue: Subpotent: Out of specification for assay at the 12-month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: methylPREDNISolone Sodium Succinate For Injection Recalled by Hikma...
The Issue: Labeling: Incorrect Instructions: Vial label incorrectly instructs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ormco Damon Q2 Orthodontic Metal Bracket Recalled by Ormco/Sybronendo Due to...
The Issue: The bracket torque was mislabeled on the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Recalled by...
The Issue: The filter installed onto the tube set may have the incorrect pore size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to Recalled by...
The Issue: Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Simulus 750 Flexible Ring/Band Accessory Kit - Product Usage:...
The Issue: Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT G3+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: Marketed without a 510(k). Abbott Point of Care has determined that it does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigiTrak XT Holter Recorder Software version number B.1 and Recalled...
The Issue: if an AAA battery is inserted in the recorder and a user attempts to start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DP-30 Digital Ultrasonic Diagnostic Imaging System Recalled by Mindray DS...
The Issue: The DP-30 displays an incorrect needle-guide bracket when used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Recalled by...
The Issue: Incorrect power of lenses than the expected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Bard Intra-abdominal Pressure Monitoring Device is composed of a...
The Issue: Leaks or disconnect near the sampling port of the Intra Abdominal Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft...
The Issue: Incorrect power of lenses than the expected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeAir Telescopic Smoke Evacuation Pencil Recalled by Stryker Instruments...
The Issue: Hairline fractures in a component could allow electrical current to arc out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telescopic Uncoated (Push Button) Recalled by Stryker Instruments Div. of...
The Issue: Hairline fractures in a component could allow electrical current to arc out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telescopic Smoke Evac Pencil Recalled by Stryker Instruments Div. of Stryker...
The Issue: Hairline fractures in a component could allow electrical current to arc out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Reaction Ring Segment Recalled by Siemens Healthcare...
The Issue: Some lots ending in "17", "18", "19", or higher may have cuvette defects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AAMI 3 ROYALSILK SURGGOWN BNS XL Recalled by Cardinal Health Due to The...
The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AAMI 3 NONREIN SCRBNURGOWN BNS L Recalled by Cardinal Health Due to The...
The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AAMI 3 NONRNF SURG GWN 2XL XLNG BNS Recalled by Cardinal Health Due to The...
The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AAMI 3 FABRIC REINF SURG GOWN XL Recalled by Cardinal Health Due to The...
The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.