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. 1,988 recalls have been distributed to District of Columbia in the last 12 months.
Showing 2041–2060 of 27,451 recalls
Recalled Item: 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...
The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Airway adapter does not meet specification and may break off when attaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Airway adapter does not meet specification and may break off when attaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.