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. 1,733 recalls have been distributed to Nebraska in the last 12 months.
Showing 48081–48100 of 49,150 recalls
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...
The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...
The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...
The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.