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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.
Showing 32921–32940 of 47,654 recalls
Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due...
The Issue: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...
The Issue: E. CAM and Symbia system with foresight detectors performing gated or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/2" x 1.5" : 20-06S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Strung 3/4" : 30-03 Product Usage: Recalled...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Policot 1/2" x 1/2" : 90-06 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 15 mm x 15 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ray-Cot 1/2" x 3" : 60-09 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 70 mm x 10090 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/2" x 1/2" : 20-04S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 3/8" x 2" : 20-26S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Uniqcot 1/2" x 1/2" : 67-06 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 5 mm x 13 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 10 mm x 13 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.