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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 43121–43140 of 47,654 recalls
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...
The Issue: Upgrade installation script is designed to overwrite the same pouch files in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...
The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benztropine Mesylate Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of particulate matter: characterized as thin colorless flakes that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...
The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...
The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nata Komplete Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NataChew Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 430 ec Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 430 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS Recalled by Priester...
The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...
Recommended Action: Do not consume. Return to store for a refund or discard.