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.

49,990 total recalls
2,591 in last 12 months

Showing 1218112200 of 28,355 recalls

Medical DeviceFebruary 13, 2020· NuVasive Inc

Recalled Item: NUVASIVE MAGEC 2 Rod X.X mm XX mm Recalled by NuVasive Inc Due to...

The Issue: Post-implantation separation of an actuator end cap component that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Insulet Corporation

Recalled Item: Omnipod DASH Personal Diabetes Manager (PDM) Recalled by Insulet Corporation...

The Issue: In certain scenarios, the Omnipod DASH PDM may suggest an inaccurate bolus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Total Bilirubin_2 assay- SMN: 10341115 (40 mL) & Recalled by...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Total Bilirubin Flex reagent cartridge -In vitro Diagnostic for...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Total Bilirubin_2 assay-In vitro Diagnostic for the...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Direct Bilirubin_2 assay-SMN: 10316610 (20 mL) & 10341114...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Total Bilirubin Flex¿ reagent cartridge -In vitro...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the Recalled by...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Microbiologics Inc

Recalled Item: Microbiologics QC SETS AND PANELS Recalled by Microbiologics Inc Due to...

The Issue: KWIKSTIK 2 Pack () and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK 2 Pack Trichosporon dermatis derived from ATCC 204094 (Catalog#...

The Issue: KWIKSTIK 2 Pack () and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific released a new Software Update Application that was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific released a new Software Update Application that was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2020· Boston Scientific Corporation

Recalled Item: Imager II 5F Angiographic Catheters Recalled by Boston Scientific...

The Issue: Potential for tip detachment of Imager II 5F Angiographic Catheters

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 11, 2020· Intellijoint Surgical, Inc.

Recalled Item: Intellijoint Navigation System Recalled by Intellijoint Surgical, Inc. Due...

The Issue: During total knee arthroplasty (TKA), the software may incorrectly calculate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: McKesson Cardiology ECG Management Recalled by CHANGE HEALTHCARE CANADA...

The Issue: Inaccurate estimation of the heart rate may occur in instances where the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Stick Sponge Presaturated W/PVP DYND70288H 2/PK Expiration Recalled...

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Sterile 3mL Syringes with 21GA x 1 Inch Needle Recalled by Medline...

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Winged Sponges Presaturated W/PVP DYND70289H Expiration 06/30/2022....

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- Recalled...

The Issue: Tomosynthesis image acquisition sequence did not stop automatically after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Recalled by Siemens Medical Solutions USA, Inc Due to The Ysio system...

The Issue: The Ysio system may process incorrect internal values for the position of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing