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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 40261–40280 of 47,654 recalls
Recalled Item: BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System...
The Issue: A portion of the BBL Crystal Enteric/Nonfermentor (E/NF) Identification kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRK QRG for the da Vinci Standard Surgical System Recalled by Intuitive...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Manual for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connection QRG for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stapler Addendum for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insert for IRK for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vision Troubleshooting Guide for the da Vinci Standard Surgical System...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cautery QRG for the da Vinci Standard Surgical System Recalled by Intuitive...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vessel Sealer QRG for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Site US Manuals and Single Site OUS Manuals for Recalled by Intuitive...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Rubber Latex QRG for the da Vinci Standard Surgical System Recalled...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vessel Sealer Addendum for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endowrist Instrument and Accessory Manual for the da Vinci Standard Recalled...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche MODULAR ANALYTICS EVO Serum Work Area (SWA) Recalled by Roche...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 analyzer series Operators Manual Roche cobas Filter label:...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isoniazid Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed...
The Issue: Failed Dissolution Specifications: Stability lots cannot support dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory...
The Issue: The interface fails to send abnormal flags for Lab test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO PACK EXTREMITY CUSTOMED CONTENTS: (1) TABLE COVER REINFORCED 50"...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAP Abdom w/pouch Customed code 900-2619 Recalled by Customed, Inc Due to...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E..N.T. PACK - (5) SPONGE TONSIL 7/8 XRD (1) TABLE Recalled by Customed, Inc...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.