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. 1,713 recalls have been distributed to District of Columbia in the last 12 months.
Showing 41901–41920 of 47,654 recalls
Recalled Item: IMMULITE/IMMULITE 1000 Systems FOL Folic Acid Recalled by Siemens Healthcare...
The Issue: potential for an accelerated decline in counts per second (CPS) for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imitrex STATdose System Recalled by GlaxoSmithKline, LLC. Due to Lack of...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets USP 0.5 mg. Rx Only Recalled by Sandoz Inc Due to Failed...
The Issue: Failed Moisture Limit; Out of Specification (OOS) results were obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sumatriptan Succinate Injection Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Actavis Elizabeth LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: During routine stability testing one tablet was found with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: sertraline HCl tablets Recalled by Greenstone LLC Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot No. and/or Exp Date: Expiration date...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEAC Advanced Dental System Recalled by ASI Medical, Inc. Due to ASI Medical...
The Issue: ASI Medical is initiating a field correction for the SEAC Advanced Dental...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 46cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 36cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC VORTX 2MM X 3MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 15MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 45 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC-10 ULTRA SOFT 2MM X 3CM Recalled by Stryker Neurovascular...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 10MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 30MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 20MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC-18 360 18MM X 30CM Recalled by Stryker Neurovascular Due...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.