Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,598 recalls have been distributed to Arkansas in the last 12 months.
Showing 12941–12960 of 49,990 recalls
Recalled Item: syngo Application software VE20 (Material Number 10848815) installed on the...
The Issue: After CT image data from Toshiba is loaded, image mirroring can occur along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor in combination with a Siemens Healthineers table Recalled...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane- in combination with a Siemens Healthineers table...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- in combination with a Siemens Healthineers table or Recalled by...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: Product is mislabeled as self-righting Luer slip tip caps, yellow.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anterior Hip Pack - Surgical Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coryell Memorial Hosp Total Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicare Neuro Pack - Neurological Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Pack - Surgical Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lum Lam Custom Pack - Anesthesia Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S Recalled by...
The Issue: Devices distributed lacked regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software model numbers: 20910-01 Recalled by Brainlab AG...
The Issue: The yaw angle may be incorrect for CBCT positioning workflows using setup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: hydrALAZINE HCl Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...
The Issue: Surgical knives may contain incorrect description printed on handles....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...
The Issue: Recalled devices were packaged in convenience kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Factor 75 - Fiery Beef & Black Bean Chili 12.7oz Recalled by FACTOR Due to...
The Issue: Undeclared Milk Allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.