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. 979 recalls have been distributed to District of Columbia in the last 12 months.
Showing 25181–25200 of 47,654 recalls
Recalled Item: Transferrin is an in vitro diagnostic assay for the quantitative Recalled by...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEAD TIP GD WIRE 3.0MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HexaPOD evo RT Couch Top (also known as HexaPOD evo Module) Recalled by...
The Issue: Upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Correction vector...
The Issue: Correction vector confirmation message is lost if access point is changed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G-PIN 2.8BL 3.2PL 60CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2MM X 510MM COCR THD TIP Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL TIP GUIDE WIRE 2.0MMX60CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL TIP GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRILL PT GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoglobulin M is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apolipoprotein A1 is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...
The Issue: If two devices are plugged into the same channel/port in the generator, both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAREstream ProNox Nitrous Oxide Delivery System labeled as the following:...
The Issue: Two analgesic gas delivery system oxygen/nitrous oxide mixers were reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silver-Zinc Throat Spray Recalled by MBi Distributing Inc. dba MBi...
The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Argentum Elixir Colloidal Silver Recalled by MBi Distributing Inc. dba MBi...
The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.