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 27261–27280 of 28,355 recalls
Recalled Item: Philips HeartStart XL M4735A Defibrillator/Monitors Recalled by Philips...
The Issue: HeartStart XL Defibrillator/Monitor (M4735A) used on a patient when AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility...
The Issue: The potential exists for the wheel to rotate freely despite engagement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: Recalled...
The Issue: Terumo Cardiovascular Systems (CVS) received two reports of the false back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc Recalled by...
The Issue: The 8 Fr. Bardex All-Silicone Foley Catheter with 3cc balloon had an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cemented Tibial Drill Product Usage: The cemented tibial drill is Recalled...
The Issue: Zimmer is initiating a recall of the Cemented Tibial Drill for the Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set with 150 mL Burette Recalled...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: materials "RETINAL OCT Analysis and Interpretation Method" shipped with...
The Issue: Devices labeled for an intended use not included in the existing 510(k) or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Polyaxial Screw...
The Issue: This action is being initiated following a detailed investigation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap...
The Issue: This action is being initiated following a detailed investigation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single...
The Issue: The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/Needles with Orthocord Product Number: 222968 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Ethibond and needles Product Number: 222960 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Fracture...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Recalled...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.