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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 12941–12960 of 27,451 recalls
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Jarit GEMINI CLAMP 9 1/4 inch - used in Recalled by Integra...
The Issue: A small crack at the box lock corner may after multiple cleaning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...
The Issue: The device data being collected and transferred to the monitoring center may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...
The Issue: A complaint was received regarding kinking of the device prior to use. If a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...
The Issue: The electrode lead connector has a protruding conductor beyond insulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder...
The Issue: Separation of front and rear barrels upon activation of the safety feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.