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 18681–18700 of 47,654 recalls
Recalled Item: Oncomine Dx Target Test DNA Control-IVD for detection of DNA Recalled by...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of Recalled by Life...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Torrent Dx No Template Control Kit- IVD for detection Recalled by Life...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncomine Dx Target Test RNA Control- IVD for detection of Recalled by Life...
The Issue: Extended Expiration Date prior to clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Recalled by...
The Issue: A high frequency output (2 MHz) has not been cleared for distribution in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips...
The Issue: There were unknown bioburden levels prior to sterilization, which may affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprout Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mixed Greens 4 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spring Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Red Clover 4 oz Recalled by Chicago Indoor Garden, Inc. Due to Potential E....
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...
The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PreludeSYNC DISTAL Radial Compression Devices Recalled by Merit Medical...
The Issue: During the sterilization of radial compression devices, some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...
The Issue: Updated Instructions For Use- to contraindications and potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...
The Issue: Intermittent failure of a signal being sent to a monitor from the touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.