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. 944 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34501–34520 of 47,654 recalls
Recalled Item: BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXTROAMPHETAMINE SACCHARATE Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: High out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ascorbic Acid 500 MG/ML Inj. Recalled by RemedyRepack Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bicillin L-A 600000 Units/mL Inj. Recalled by RemedyRepack Inc. Due to...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin B-Complex 100 Recalled by RemedyRepack Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam 2 mg/mL Inj. Recalled by RemedyRepack Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Humulin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novolin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocuronium Bromide 50 MG/5ML INJ. Recalled by RemedyRepack Inc. Due to...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.