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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 9101–9120 of 27,451 recalls
Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...
The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...
The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...
The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...
The Issue: Missing splash guard which may expose users to hazardous materials. .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX Delta Mod Head Recalled by Corin Ltd Due to The packaging...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.