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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.
Showing 1161–1180 of 27,451 recalls
Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...
The Issue: Blood collection tubes were manufactured with the label applied too high on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argus PB-3000 Recalled by Schiller, Ag Due to Vital sign monitoring...
The Issue: Vital sign monitoring instrument may trigger an error message during blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...
The Issue: Software issue that results in the display of outdated information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 12A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 7 Recalled...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 2023B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...
The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code:...
The Issue: As a result of Post-Market half-time stability testing, false negative test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000....
The Issue: Reports of out-of-box failures discovered during the limited launch phase....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019....
The Issue: Potential for undetected, deformed a-traumatic tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reef TA Inserter Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to...
The Issue: Inserter, used as part of a system with an intervertebral body fusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...
The Issue: The catheters may not retain their shape.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...
The Issue: The catheters may not retain their shape.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.