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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3821–3840 of 27,451 recalls
Recalled Item: KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R Recalled by American Contract...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJOR KNEE - 302497- Procedure tray Catalog Number: ASKN23B Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S Recalled...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE - 297835-Procedure Kit Catalog Number: RGTK10K Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOWER EXTREMITY - 247542- Procedure tray Catalog Number: BFLE56X Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL Recalled by American Contract Systems Inc Due to Ethylene Oxide/Ethylene...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...
The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 Recalled by...
The Issue: The firm received reports that some blood collection tubes have experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate...
The Issue: Kit assigned an extended expiration date of 24-Jul-2025 during release. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Initial Placement Dilator Set. Used to place gastrostomy devices....
The Issue: Devices were labelled with the incorrect guidewire labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical Inc Due to The...
The Issue: The smaller chamber of the two chamber bag is bursting when nurses are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile Recalled by SVS LLC Due to Mislabeling
The Issue: Firm received complaints regarding skin irritation when using the gloves,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...
The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.