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. 2,496 recalls have been distributed to District of Columbia in the last 12 months.
Showing 17841–17860 of 27,451 recalls
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...
The Issue: Product shipped proximate to or past the expiration date listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...
The Issue: Surgical technique was revised to prevent static plate screws blocking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software changes now available to address several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...
The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software changes now available to address several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed that in isolated cases when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...
The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.