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 25741–25760 of 28,355 recalls
Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...
The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to the white printed paper...
The Issue: the white printed paper layer on the pouch packaging may not be fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1) Asnis III Cannulated Screw 4.0x40mm TL Recalled by Stryker...
The Issue: Stryker received a report that the length of the cannulated screw asnis III,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the footswitch cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pCO2 D788 Membranes. Distributed by Radiometer America Recalled by...
The Issue: RADIOMETER has become aware that some D788 pCO2 membranes can cause biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Reservoirs Recalled by Medtronic MiniMed Due to...
The Issue: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...
The Issue: Upgrade installation script is designed to overwrite the same pouch files in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...
The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER Recalled by Ecolab Inc...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...
The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...
The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.