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. 2,623 recalls have been distributed to Arkansas in the last 12 months.
Showing 8941–8960 of 49,990 recalls
Recalled Item: OEC 9800 Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of...
The Issue: Potential for lot number discrepancies between the test strip packaging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASCORBIC ACID PRESERVED INJECTION SOLUTION Recalled by Empower Clinic...
The Issue: Mislabeling: preservative free product labeled as preserved.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline O.R. Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The scissors were manufactured without a tip protector resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Icelock 125 Ratchet Recalled by Ossur H / F Due to A mechanical lock used to...
The Issue: A mechanical lock used to connect and release a locking liner into a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Driver Instrument Recalled by Boston Scientific Neuromodulation Corporation...
The Issue: Pending update to indirect decompression system instructions for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial Recalled by Revive Rx...
The Issue: Sub-potent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.