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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 46381–46400 of 47,654 recalls
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stat-Check Resuscitator Recalled by Ventlab Corporation Due to Possible...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Adult Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034...
The Issue: When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR220amx Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromovision High Definition (HD) Wireless Camera Recalled by Berchtold...
The Issue: Defective camera: There is a possibility that the connection of the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...
The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.137 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.112 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.125 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.