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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 41181–41200 of 47,654 recalls
Recalled Item: Queso Fresco Amigo Brand Round Fresh Cheese Recalled by Roos Foods Inc Due...
The Issue: Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Santa Rosa de Lima Queso de Huerta (Fresh Cheese) Recalled by Roos Foods Inc...
The Issue: Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Santa Rosa de Lima Mantequilla de Bolsa Tradicion Centroamericana Recalled...
The Issue: Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mexicana Brand Queso Fresco Fresh Cheese Recalled by Roos Foods Inc Due to...
The Issue: Samples of Santa Rosa De Lima Cuajada en Terron (fresh curd cheese) were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...
The Issue: The bar code that is printed on the Master Carton label does not correspond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newman's Own Salsa Con Queso Recalled by Newman'S Own Inc. Due to Undeclared...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...
The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Vancomycin 30 mcg Recalled by Remel Inc Due to Some of the discs may...
The Issue: Some of the discs may not be impregnated with the antibiotic.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...
The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...
The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: A component of the MRx Processor Board may be susceptible to damage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...
The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...
The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...
The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...
The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...
The Issue: Chemical Contamination: The recalling firm received notice that their...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...
The Issue: Presence of Particulate Matter: Potential for small black particles to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.