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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18641–18660 of 47,654 recalls
Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew FOOTPRINT Ultra PK Suture Anchor Recalled by Smith & Nephew,...
The Issue: Space between the device and the packaging permits excessive movement which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner...
The Issue: RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.