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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3841–3860 of 27,451 recalls
Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...
The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeos Robotic Digital Microscope Recalled by Aesculap Inc Due to Possibility...
The Issue: Possibility of the robotic arm to drop more than 10cm from its original...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO CBC Test Kit Recalled by SIGHT DIAGNOSTICS LTD Due to One Test Kit...
The Issue: One Test Kit lot (TK1-10114) shows a positive bias in the platelet count due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring System Recalled by Draeger...
The Issue: Device is not in full compliance to Type CF requirements of IEC 60601-1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in...
The Issue: The reason for recall is the meters may show an incorrect measurement unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Darby Prophylaxis Paste with 1.23% Fluoride Ion Recalled by Young Dental...
The Issue: Part number 040032, Lot number, 248607 was incorrectly labeled as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica HistoCore Arcadia H Recalled by LEICA BIOSYSTEMS NUSSLOCH GMBH Due to...
The Issue: An issue with safe usage of the device was identified whereby toxic smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda Intrathecal Catheter Recalled by Medtronic Neuromodulation...
The Issue: Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in Recalled...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONOCRYL (poliglecaprone 25) Suture - Intended for use in general Recalled...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL (polyglactin 910) Suture - Indicated for use in general Recalled by...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II (polydioxanone) Suture - Intended for use in general Recalled by...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...
The Issue: The wrong configuration of the blade was in the package. The bevel was on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...
The Issue: The wrong configuration of the blade was in the package. The bevel was on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...
The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.