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. 2,567 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14381–14400 of 27,451 recalls
Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...
The Issue: Potential for external blood leaks from the dialyzer header
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...
The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...
The Issue: The firm has detected a potential risk using the command. After releasing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...
The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...
The Issue: Experienced accelerated battery depletion and a shortened replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...
The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...
The Issue: The firm has become aware that due to a chemical reaction, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...
The Issue: An incorrect test result for a single analyte may have been reported for up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...
The Issue: Screw is missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...
The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.