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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 29221–29240 of 47,654 recalls
Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...
The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS Recalled by...
The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol (17-B-Estradiol Recalled by Spectrum Laboratory Products, Inc. Due...
The Issue: CGMP Deviations: these repackaged and redistributed products are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...
The Issue: CGMP Deviations: these repackaged and redistributed products are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...
The Issue: An unexpected transient mode switch behavior was detected by Medtronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...
The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI . The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...
The Issue: An extremely dusty computer can cause problems at system start, or rarely,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...
The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Bakery Peanut Butter Chocolate Chunk Cookies Recalled by Jimmy's Cookies...
The Issue: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional...
The Issue: Potential Patient Demographic Error with Blank Patient ID Field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys PreciControl Varia 3 Recalled by Roche Diagnostics Corporation Due...
The Issue: e-barcode and value sheet for PreciControl Varia contains a typographical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.