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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16021–16040 of 27,451 recalls
Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000 US) G46022 is...
The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...
The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The...
The Issue: CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...
The Issue: Sterility failure found in one of the units in the lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...
The Issue: Product is labeled with "CE", but is not yet approved in the European Union.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...
The Issue: The power supply unit may be damaged and may fail to start up when the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...
The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable...
The Issue: An EEPROM chip error code may occur when the catheters are used with CARTO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Free Thyroxine (FT4L) Flex¿ reagent cartridge Recalled by Siemens...
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Folate (FOL) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi 3g Allergy specific IgE Universal Kit...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.