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. 1,053 recalls have been distributed to Arkansas in the last 12 months.
Showing 14761–14780 of 49,990 recalls
Recalled Item: GaviLyteTM - C PEG-3350 (240g) and Electrolytes for Oral Solution Recalled...
The Issue: Failed Stability Specification; Out of specification for Osmolarity
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethosuximide Oral Solution USP 250 mg/5 mL Recalled by PAI Holdings, LLC....
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection 100 mg/mL Recalled by Teva Pharmaceuticals...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprostadil Injection USP Recalled by Teva Pharmaceuticals USA Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amikacin Sulfate Injection USP 1 gram/4mL (250mg/ML) Recalled by Teva...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...
The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...
The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...
The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity Screw Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...
The Issue: Missing splash guard which may expose users to hazardous materials. .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity Dual Mobility Recalled by Corin Ltd Due to The packaging...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity Liner ECIMA Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Test strip vials may open while inside sealed cartons during shipment. An...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.