Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,439 recalls have been distributed to Nebraska in the last 12 months.
Showing 27041–27060 of 28,140 recalls
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: 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: 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: 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 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: 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 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 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: 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: SpiraLok 6.5mm with Ethibond and needles Product Number: 222962 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: 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: Sterile Recalled by Gynex Corporation Due to The wrong electrical connector...
The Issue: The wrong electrical connector pin was attached to the cord during assembly...
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: 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 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 5.0mm with Panacryl and needles Product Number: 222961 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 5.0 w/out Needles with Orthocord Product Number: 222969 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 6.5mm with Panacryl and needles Product Number: 222963 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.