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. 2,538 recalls have been distributed to Nebraska in the last 12 months.
Showing 16561–16580 of 28,140 recalls
Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...
The Issue: if the cables of the Monica IF24 System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...
The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...
The Issue: Product reportedly shutting down during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Access Set Recalled by Boston Scientific Corporation Due to...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malecot Nephrostomy Catheter System Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: digital x-ray detector ProGrade R1 - solid state X ray Recalled by Philips...
The Issue: It the WiFi connection between the SkyPlate detector and HP transfer point...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synvisc-One ¿ (hylan G-F 20) Recalled by Sanofi Genzyme Due to Contamination...
The Issue: Contamination with Methylbacterium thiocyanatum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is Recalled...
The Issue: Potential polymer material degradation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and Recalled...
The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c16000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...
The Issue: The serum may fail to agglutinate within the specified minimum reaction time.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...
The Issue: Potential for the display processor to experience an unexpected failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.