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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 42481–42500 of 47,654 recalls
Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...
The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...
The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...
The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...
The Issue: Integra LifeSciences has identified through an internal evaluation that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL PF Recalled by Avella of Deer Valley, Inc. Due...
The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.