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. 2,591 recalls have been distributed to Arkansas in the last 12 months.
Showing 13241–13260 of 28,355 recalls
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Medical X-ray Imaging System Recalled by Shanghai United Imaging...
The Issue: X-ray imaging system positioning image and protocol label is reversed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce GX560 monochrome LCD monitor Recalled by Eizo Corporation Due to...
The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX360 Recalled by Eizo Corporation Due to Under certain...
The Issue: Under certain conditions, a marble pattern infrequently appears on the monitor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000...
The Issue: Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan/CF: a) 3.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan/HVT: a) 5.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan Preformed: a) 3.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan Uncuffed: a) 2.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan LTS: a) 4.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan/HVT Novaplus: a) 7.0 mm Recalled by Teleflex Medical Due to...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to Reported...
The Issue: Reported complaints indicate an increased incidence of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System...
The Issue: Artis zee/Q systems patient tables may potentially have cracks in the table...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Body Weight Support (BWS) Light Recalled by MOTEK MEDICAL B.V. Due to The...
The Issue: The firm discovered a potential manufacturing deviation of the yoke of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTILITE IgM Kit Recalled by The Binding Site Group, Ltd. Due to There is a...
The Issue: There is a potential that users may experience difficulty validating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.