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. 2,451 recalls have been distributed to Arkansas in the last 12 months.
Showing 26521–26540 of 28,355 recalls
Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Risk that air...
The Issue: Risk that air may be introduced into the device which may lead to an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Cube Pessary 1 5/8"" Recalled by Cooper Surgical, Inc. Due...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare SpO2RT2 bed. Product Usage: Bed Recalled by Hill-Rom, Inc. Due to...
The Issue: In certain situations a software problem with the TotalCare SpO2RT¿ 2 bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Gellhorn Flexible Pessary 3" Recalled by Cooper Surgical,...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Incontinence Ring Flexible Pessary #4 Recalled by Cooper...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Cube Pessary w/Drainage Holes #0"1" Recalled by Cooper...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Incontinence Dish Folding Pessary #0 Recalled by Cooper...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Incontinence Dish Folding Pessary #0 Recalled by Cooper...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTIO Inc. Recalled by Intio Inc Due to INTIO Inc. distributed a SVM User's...
The Issue: INTIO Inc. distributed a SVM User's Manual and it has an editing mistake...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Incontinence Dish w/ Support Pessary #5 Recalled by Cooper...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Gellhorn Flexible Pessary -2 3/4" Recalled by Cooper...
The Issue: Pessary mislabeled outer package may not the size of the product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMO-402 Mononucleosis Rapid Test Device (Whole Blood/Serum/Plasma). Catalog...
The Issue: Alere San Diego is recalling the Clearview Mononucleosis Cassette because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.