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. 2,635 recalls have been distributed to District of Columbia in the last 12 months.
Showing 4541–4560 of 27,451 recalls
Recalled Item: Centurion PICC LINE SECUREMENT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE M1S0179 STRL TAPE/PEN PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion STERILE TRACH BRUSH Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion STERILE #16 RUBBER BAND Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altair 330 lbs w/o Hanger Bar Recalled by Human Care Hc Sweden Ab Due to...
The Issue: Patient lift hanger bar may come loose, which could potentially pose risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Software Version Numbers version numbers 8B Recalled by RAYSEARCH...
The Issue: A use error that has occurred with RayStation/RayPlan, where material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...
The Issue: Calibration Buttons being used in the kitting process were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE SWABSTICKS PVP 3 PK Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 1.0 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...
The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...
The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...
The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Thoracic Stent-Graft System Recalled by Bolton Medical Inc. Due to...
The Issue: The stent-graft inside the delivery system was the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.