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. 2,629 recalls have been distributed to District of Columbia in the last 12 months.
Showing 6221–6240 of 47,654 recalls
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betimol (timolol ophthalmic solution) 0.5% Recalled by Thea Pharma, Inc. Due...
The Issue: Lack of Assurance of Sterility: Out of specification for volume and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: Beckman Coulter manufacturing discovered cracks around a threaded insert on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:connect mobile app used in conjunction with t:slim X2 insulin Recalled by...
The Issue: During normal use, the mobile app version 2.7 may crash and be automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml...
The Issue: Randox Laboratories has identified that Inorganic Phosphate in Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There...
The Issue: There are two windows on the test device, the control line window and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There...
The Issue: There are two windows on the test device, the control line window and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neria Soft Infusion Set Recalled by Unomedical A/S Due to Specific lots of...
The Issue: Specific lots of Neria Soft Infusion Sets, which have been shipped into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bed Assist Bars Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline is recalling certain lots of our Adult Portable Bed Rails that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bed Assist Bars Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline is recalling certain lots of our Adult Portable Bed Rails that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface Recalled by Baxter Healthcare Corporation Due...
The Issue: Inconsistencies were identified with service records associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiji Natural Artesian Water 500 mL (24 pack) Case Recalled by Natural Waters...
The Issue: Firm testing revealed Manganese in addition to three bacterial genera.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Treprostinil Injection Recalled by Par Sterile Products LLC Due to Presence...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Digoxin Tablets Recalled by Novitium Pharma LLC Due to Cross Contamination...
The Issue: Cross Contamination with Other Products:(mycophenolate mofetil).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Febuxostat Tablets 80mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Febuxostat Tablets 40mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...
The Issue: There is a risk of mistreatment as irradiation is not prevented when some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.