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. 1,026 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14141–14160 of 47,654 recalls
Recalled Item: Karl Storz Udel Sterilization Tray Instructions for Use Recalled by Karl...
The Issue: To ensure sterilization effectiveness, sterilization tray instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPL Coupling Gel Recalled by Lumenis, Inc. Due to Ultrasound gels and...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: These are communication systems Recalled by Hill-Rom Inc. Due to An...
The Issue: An unrecoverable error may occur where a component will fail to complete the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 Recalled by...
The Issue: When the ultrasound system is used in combination with a Fujifilm (formally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to Top label of the outer...
The Issue: Top label of the outer package of the collection kit Item 5820-3118 showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR Recalled by SEDECAL SA Due to While cleaning or...
The Issue: While cleaning or disinfecting the system, if the process is not followed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 Recalled by KEURIG DR PEPPER...
The Issue: The company has received off flavor and off aroma complaints identified with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Target Good & Gather Mixed Berry Sparkling Water 8 pack Recalled by KEURIG...
The Issue: The company has received off flavor and off aroma complaints identified with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Target Good & Gather Coconut Pineapple Sparkling Water 8 pack Recalled by...
The Issue: The company has received off flavor and off aroma complaints identified with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Polar Black Cherry Premium Seltzer 12 pack of 12oz cans Recalled by KEURIG...
The Issue: The company has received off flavor and off aroma complaints identified with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Skinny Needle with Chiba Tip. RPN 090010 Recalled by Cook Inc. Due to...
The Issue: Specific lots may contain black debris on the exterior of the inner stylet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL ReadiPlasTin (20 mL) Recalled by Instrumentation Laboratory Due to...
The Issue: The firm has received customer reports of performance issues with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.