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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18921–18940 of 27,451 recalls
Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...
The Issue: "We have received reports of patients hair being caught in the e.cam and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...
The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome without LeMills Recalled by LeMaitre...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.:...
The Issue: Siemens Healthcare Diagnostics determined that the Dimension Vista Calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDIA¿ 60cc Piston Irrigation Syringe Recalled by C.R. Bard, Inc. Due to...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ Piston Syringe Recalled by C.R. Bard, Inc. Due to Package Defect:...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ 70cc Piston Syringe with Catheter Tip Recalled by C.R. Bard, Inc. Due...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ Irrigation Recalled by C.R. Bard, Inc. Due to Package Defect: Products...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....
The Issue: Tip Breakage at the glue joint between the obturator body and tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 Recalled by Becton...
The Issue: A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase (Colorimetric) Product Usage: A lipase test system is Recalled...
The Issue: According to the firm carry over was observed when the Lipase test is run...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.Plaza VB 10 A Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Recalled...
The Issue: Incorrect expiration date on the magnetic strip that does not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Plaza picture archiving and communication system (PAC) (PACS) intended...
The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certegra Workstation used in conjunction with Medrad Stellant CT Injection...
The Issue: CertegraWorkstation when used in conjunction with the Medrad Stellant CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....
The Issue: Tip Breakage at the glue joint between the obturator body and tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion...
The Issue: Siemens became aware of a potential issue with the patient table for Ysio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.