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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 25561–25580 of 27,451 recalls
Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...
The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...
The Issue: A defect on the master-side connector block of the pneumatic tool changer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...
The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....
The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...
The Issue: The recall was initiated because Shimadzu Corporation has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...
The Issue: There was an occurrence where the patient case data did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrea¿ CT Brain Perfusion made available in various configurations under...
The Issue: Vital Images, Inc. (Vital Images) received one report about potential user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...
The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.