Nebraska recalls
4319 federal recalls on file affecting Nebraska - 334 Nebraska-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline Lumbar Puncture Kit recalled for Lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline medical kits recalled for Lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline convenience kits recalled for lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline procedure kits recalled for defective lidocaine
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline suturing kits recalled for Lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline biopsy kits recalled for lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for Lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline central line kits recalled for defective lidocaine
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for Lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline epidural kits recalled for lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceMedlineClass IINationwideMedline arterial kits recalled for Lidocaine quality issues
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
- 2026-07-08FDA-DeviceHamilton Medical AGClass INationwideHamilton Medical ventilator breathing circuits recalled for valve obstruction risk
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result in "exhalation obstructed " alarm, which may result in inadequate ventilation, oxygen desaturation. Advising: Prior to use, test lung action. If alarm occurs, expiratory valve set removal to overcome membrane adhesion or replacement
- 2026-07-08FDA-FoodNara OrganicsClass INationwideNara Organics infant formula recalled for botulism risk
Product may be contaminated with Clostridium botulinum.
- 2026-07-08FDA-FoodMARS SNACKINGClass IIMorningStar Farms sausage patties recalled for plastic contamination risk
Potential contamination with plastic material
- 2026-07-08FDA-FoodMARS SNACKINGClass IIMorningStar Farms vegan nuggets recalled for plastic contamination risk
Potential contamination with plastic material
- 2026-07-08FDA-FoodMOGO Moringa LLCClass INationwideMOGO Pure Moringa capsules recalled for Salmonella risk
Product may be contaminated with Salmonella Typhimurium
- 2026-07-08FDA-DrugCiplaClass IINationwideCipla Cinacalcet tablets recalled for N-nitroso impurity
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
- 2026-07-08FDA-DrugCiplaClass IINationwideCipla Cinacalcet tablets recalled for N-nitroso impurity
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
- 2026-07-08FDA-DrugCiplaClass IINationwideCipla Cinacalcet tablets recalled for impurity risk
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
- 2026-07-08FDA-DrugLannettClass IINationwideLannett amphetamine capsules recalled for labeling mix-up
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
- 2026-07-08FDA-DrugAsclemed USA Inc.Class IINationwideAsclemed Lidocaine HCl Injection recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-08FDA-DrugAsclemed USA Inc.Class IINationwideAccucaine lidocaine injection recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-08FDA-DrugACCORD HEALTHCARE, INC.Class IINationwideAccord levothyroxine tablets recalled for subpotency
Subpotent Drug
- 2026-07-08FDA-DrugLupinClass IINationwideLupin prednisolone acetate eye drops recalled for foreign substance
Presence of Foreign Substance
- 2026-07-08FDA-DrugACCORD BIOPHARMA INCClass IINationwideAccord BioPharma IMULDOSA injection recalled for sterility concerns
Lack of assurance of Sterility:
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD ChloraPrep CLear recalled for sterility assurance issue
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD ChloraPrep CLear recalled for unsterilized applicators
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD ChloraPrep Scrub Teal recalled for sterility concerns
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD ChloraPrep Scrub Teal recalled for sterility risk
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
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