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. 2,612 recalls have been distributed to District of Columbia in the last 12 months.
Showing 10241–10260 of 47,654 recalls
Recalled Item: Humatrix Microclysmic Gel Recalled by Consolidated Chemical, Inc Due to CGMP...
The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Techni-Care Chloroxylenold 3% Recalled by Consolidated Chemical, Inc Due to...
The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) Recalled by THE ISH...
The Issue: undeclared soy proteins
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Tablets Recalled by MACLEODS PHARMA USA, INC Due to Mismatching...
The Issue: Mismatching of the embossing on the tablets (T7) with the embossing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...
The Issue: Incorrect expiration date on product label. The manufacturing date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SINUVA (mometasone furoate) sinus implant Recalled by Intersect ENT, Inc....
The Issue: Failed Dissolution Specification; product did not meet the average 24-hour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...
The Issue: Firm identified that user may be unable to adjust the length of the Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter...
The Issue: Due to the adhesive provided within the catheter repair kits maybe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR Recalled by...
The Issue: Gauge malfunction: Digital gauge displays an incorrect tank pressure -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuadMix Plus (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine)...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.