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 1232112340 of 28,355 recalls

Medical DeviceJanuary 13, 2020· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: DP-30 Digital Ultrasonic Diagnostic Imaging System Recalled by Mindray DS...

The Issue: The DP-30 displays an incorrect needle-guide bracket when used with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· CooperVision Inc.

Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Recalled by...

The Issue: Incorrect power of lenses than the expected

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· C.R. Bard Inc

Recalled Item: The Bard Intra-abdominal Pressure Monitoring Device is composed of a...

The Issue: Leaks or disconnect near the sampling port of the Intra Abdominal Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· CooperVision Inc.

Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft...

The Issue: Incorrect power of lenses than the expected

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: SafeAir Telescopic Smoke Evacuation Pencil Recalled by Stryker Instruments...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Telescopic Uncoated (Push Button) Recalled by Stryker Instruments Div. of...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Telescopic Smoke Evac Pencil Recalled by Stryker Instruments Div. of Stryker...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Reaction Ring Segment Recalled by Siemens Healthcare...

The Issue: Some lots ending in "17", "18", "19", or higher may have cuvette defects...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 ROYALSILK SURGGOWN BNS XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREIN SCRBNURGOWN BNS L Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONRNF SURG GWN 2XL XLNG BNS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRIC REINF SURG GOWN XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-REINF SURG GOWN LG 2 TWL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREINF SURGICAL GOWN 4XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRNF SCRUB SURG GWN XL NS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: ROYALSILK 3XLARGE/XLONG NS Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: ROYALSILK 3XLARGE/XLONG Recalled by Cardinal Health Due to The gowns contain...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-REINF SURGICAL GOWN XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: ROYALSILK LARGE Recalled by Cardinal Health Due to The gowns contain an...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABREINF SCRUB SURG GWN L NS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing