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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 31341–31360 of 47,654 recalls
Recalled Item: Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised...
The Issue: The connector may disconnect from the tracheostomy tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS 1-Piece IOL with the TECNIS iTec Preloaded Delivery System Recalled...
The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1 Dissection Tool - 3mm CRS DBALL Recalled by The Anspach Effort, Inc. Due...
The Issue: The firm discovered on March 4, 2016 that several product codes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS OptiBlue 1-Piece Intraocular Lens (IOL) Recalled by Abbott Medical...
The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dietary Supplement Acidophilus Blend Recalled by Complete Packaging &...
The Issue: Nature's Power Solutions Acidophilus Blend due to undeclared milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: St¿ckert S5 System Recalled by Sorin Group USA, Inc. Due to Sorin/LivaNova...
The Issue: Sorin/LivaNova is initiating a field correction on the S5 Heart-lung machine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation)...
The Issue: Products contain international package insert and not the correct USA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension IRON Flex reagent cartridges Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has become aware of deferoxamine interference...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation)...
The Issue: Products contain international package insert and not the correct USA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Xhibit Telemetry Receiver (XTR) Recalled by Spacelabs...
The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...
The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista IRON Flex reagent cartridges Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has become aware of deferoxamine interference...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.2 Micron Filter Recalled by Baxter Corporation Englewood Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences has been notified of a medical device recall by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...
The Issue: Misbranded: Incorrect etching on the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...
The Issue: Siemens received multiple customer complaints indicating an increase in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.