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. 2,535 recalls have been distributed to Arkansas in the last 12 months.
Showing 17861–17880 of 28,355 recalls
Recalled Item: Drill Bit Quick-Connect Calibrated 3-Fluted 2.5 mm Diameter 230 mm Length...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...
The Issue: Listeria monocytogenes contamination of non-sterile plated media
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate System Cannulated Drill Standard...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Quick-Connect 4.5 mm Diameter 145 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill Bits 1.1 mm Diameter Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Quick-Connect 2.5 mm Diameter 110 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Distal Drill 3.2 mm Diameter Pilot Tip Recalled...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 4.5 mm...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill bit Quick-Connect 3-Fluted 2.5 mm Diameter 180 mm Length Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech 1.5" Novation Calcar Planer Guide Tip To assist the Recalled by...
The Issue: The firm determined that the labeling (surgical technique) should be updated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIGENT Creatinine (Enzymatic) Recalled by Sentinel CH SPA Due to Reagent...
The Issue: Reagent 1 component may result in Quality Control values shifting out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETRA II Programmable Infusion Pump Recalled by Flowonix Medical, Inc....
The Issue: Flowonix Medical received a report of a patient implanted with the Prometra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended...
The Issue: Olympic Pasteurmatic 3000/3500 Systems are recalled because they do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT540 X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery Ml X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lightspeed RT16 X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery Ml DR X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IQ X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis FDP Latex Reagent Recalled by Fisher Diagnostics Due to...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.