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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 31641–31660 of 47,654 recalls
Recalled Item: JUST Blueberry Muffin Mix Recalled by Hampton Creek Foods Due to Potential...
The Issue: Firm received a positive test result for Salmonella in Coconut Milk powder...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JUST Cinnamon Roll Coffee Cake Mix Recalled by Hampton Creek Foods Due to...
The Issue: Firm received a positive test result for Salmonella in Coconut Milk powder...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: COMFORT SHIELD (dimethicone) Barrier Cream Cloths Recalled by Sage Products...
The Issue: Microbial Contamination of Non-Sterile Products: contamination with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COMFORT SHIELD (dimethicone) Barrier Cream Cloths Recalled by Sage Products...
The Issue: CGMP Deviations: potential contamination of products manufactured on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 2% Chlorhexidine Gluconate* Cloth Recalled by Sage Products LLC Due to CGMP...
The Issue: CGMP Deviations: potential contamination of products manufactured on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amikacin Sulfate Injection Recalled by Teva Pharmaceuticals USA Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amikacin Sulfate Injection Recalled by Teva Pharmaceuticals USA Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by Gel Spice Co....
The Issue: Ground Turmeric may contain excess levels of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Desoximetasone Gel USP Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: product was out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...
The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...
The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...
The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...
The Issue: If an affected Patient Monitor has been powered on continuously for several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz Recalled by La...
The Issue: Calcium caseinate is declared on the label, but milk is not listed.
Recommended Action: Do not consume. Return to store for a refund or discard.