State

Nebraska product recalls

73,576 recalls have nationwide distribution and so reach Nebraska. 4,576 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total: 4,576
Critical: 715
Severe: 1,343
Most recent: 2026-10-14

Of the 4,576 recalls naming Nebraska we have scored against our rubric, 715 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,343 (29%) are Severe.

Which agencies issued them

These figures cover only the 4,576 recalls whose distribution notice names Nebraska specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

226–250 of 78152

SevereFDA (Devices)·Z-3331-2026·2026-10-07
Penumbra RED 62 Reperfusion Catheter Recalled for Fracture Risk
Penumbra Inc. is recalling 43 RED 62 Reperfusion Catheters due to manufacturing issues that may cause the catheters to fracture.
Product
Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (RED 62 Reperfusion Catheter) Model/Catalog Number: THNDRRED62SKIT Software Version: N/A Product Description: Product common name: Percutaneous catheter A complete product description…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0876-2026·2026-10-07
Par Health Recalls Buprenorphine Hydrochloride Injection Due to Crystallization
Par Health USA is voluntarily recalling 154,210 bottles of Buprenorphine Hydrochloride Injection due to crystallization. The FDA classifies this as a Class II recall.
Product
BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3294-2026·2026-10-07
FDA Recalls Medical Kits with Contaminated Pericare Wipes
American Contract Systems Inc. is recalling 1,804 medical kits containing BD CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL HYSTERECTOMY - 205989 Model No. MHAH55AM LAVH-LAP COLON Model No. SPLL54U VAG HYST PACK Model No. SPVH62P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3302-2026·2026-10-07
Heraeus Medical Recalls PALACOS R+G pro Bone Cement Due to Leakage Risk
Heraeus Medical GmbH is recalling PALACOS R+G pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall affects 59,660 units distributed worldwide.
Product
PALACOS R+G pro 40; PALACOS R+G pro 80. Model/Catalog Number: 5081288; 5081289. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3293-2026·2026-10-07
Recall of Medical Convenience Kits with Contaminated Pericare Wipes
American Contract Systems Inc. is recalling 1,804 medical convenience kits containing potentially contaminated perineal care wipes. The contamination may cause skin irritation or increase infection risk.
Product
Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays CARDIAC HEART BUNDLE NS Model No. LMCH99P OPEN HEART 2 RCH¿ 0248495 Model No. RCOH62C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3324-2026·2026-10-07
Percussionaire Travel Air and Phasitron 5 Recall for Anesthetic Warning
Percussionaire Corporation is recalling Travel Air and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Product
Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3296-2026·2026-10-07
Cardinal Health Recalls Presource Packs Due to Potential Handpiece Leakage
Cardinal Health 200, LLC is recalling 344 Presource Packs containing Stryker tube sets because handpieces may leak fluid, creating a slip and fall hazard.
Product
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT,GU DAVINCI , Catalog Number: PGVMDVBWU; 2) KIT,GU DAVINCI , Catalog Number: PGVMDVBWV; 3) KIT,GU DAVINCI , Catalog Number: PGVMDVB26; 4) KIT,GU DAVINCI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3301-2026·2026-10-07
Heraeus Medical Recalls PALACOS R pro Bone Cement Due to Leakage Risk
Heraeus Medical is recalling PALACOS R pro 40 and 80 bone cement because of a potential for monomer liquid leakage. The recall affects 33,727 units distributed worldwide.
Product
PALACOS R pro 40; PALACOS R pro 80. Model/Catalog Numbers: 5081286; 5081287. Radiopaque, poly (methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3291-2026·2026-10-07
FDA Recalls Opportunity Pro Nitrile Gloves Due to Manufacturing Defects
American Nitrile Operations LLC is recalling 17,481,000 Opportunity Pro nitrile gloves nationwide due to defects like tears and debris that may expose users to pathogens or chemicals.
Product
Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800, 72-50801,72-50802,72-50803,72-50804 Product Description: Blue Nitrile patient examination glove
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3295-2026·2026-10-07
Cardinal Health Recalls Stryker StrykeFlow PS and AHTO Tube Set Kits
Cardinal Health is recalling 3,677 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because handpieces may leak fluid, creating a slip and fall hazard.
Product
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2) KIT, LAP CHOLE , Catalog Number: PGCGLCBAD; 3) KIT, LAP CHOLE , Catalog Number: PGCGLCBAE; 4) KIT, LAP CHOLE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3304-2026·2026-10-07
Heraeus Medical Recalls PALACOS MV Pro Bone Cement Due to Leakage Risk
Heraeus Medical is recalling PALACOS MV pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall covers all lot numbers distributed worldwide.
Product
PALACOS MV pro 40; PALACOS MV pro 80. Model/Catalog Number: 5150633; 5150635. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3277-2026·2026-10-07
United Imaging uCT 530 CT Systems Recalled for Software Visibility Issue
Shanghai United Imaging Healthcare is recalling four uCT 530 CT systems due to a software defect that may hide patient images, potentially requiring rescans.
Product
Computed Tomography X-ray System, Model: uCT 530 with software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3275-2026·2026-10-07
Bard EnCor EnCompass Breast Biopsy System Software Recall
Bard Peripheral Vascular Inc is recalling 99 EnCor EnCompass Breast Biopsy and Tissue Removal Systems due to software errors that may interrupt procedures.
Product
EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number: ENCPDRIVER) with software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3305-2026·2026-10-07
Embosphere Microspheres Recalled Due to Packaging Sterility Concerns
Merit Medical Systems is recalling Embosphere microspheres because packaging holes may compromise sterility, posing an infection risk.
Product
Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, REF: S420GH/EUA, S620GH/EUA; Embosphere 700-900 micrometer 2 mL Syringe Sterile Steam, REF: S820GH/CAB; Embosphere 900-1200 micrometer 2 mL Syringe Sterile Steam, REF: S1020GH/C, S1020GH/EUA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3271-2026·2026-10-07
Alere hCG Pregnancy Test Cassettes Recalled for False Positive Results
Alere San Diego is recalling hCG rapid test cassettes because they may detect low hormone levels, leading to false positive pregnancy results.
Product
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part: FHC-A102/92210; Fisher Scientific Sure-Vue Serum/Urine¿hCG-STAT, Model/ Part: FHC-A202/23900531, FHC-A202/23900530; McKesson CONSULT Diagnostics hCG Urine…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3323-2026·2026-10-07
Percussionaire Impulsator and Phasitron 5 Recall for Anesthesia Warning Update
Percussionaire Corporation is recalling Impulsator and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Product
Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with Instruction Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3330-2026·2026-10-07
Tandem t:slim iOS App Recall Due to CGM Pairing Failure
Tandem Diabetes Care is recalling a beta version of its t:slim iOS app because it fails to pair with Abbott FreeStyle Libre 3 Plus sensors, forcing users into manual mode.
Product
Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application, iOS Model/Catalog Number: iOS software version 2.13 Software Version: iOS software version 2.13 UDI-DI: 00389152470740 Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3335-2026·2026-10-07
Siemens Atellica CH C-Reactive Protein Reagent Recalled for Falsely Elevated Results
Siemens Healthcare Diagnostics is recalling Atellica CH Revised C-Reactive Protein reagent due to the potential for falsely elevated test results.
Product
Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3289-2026·2026-10-07
FDA Recalls Performance Pro Nitrile Gloves Due to Defects
American Nitrile Operations is recalling Performance Pro blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
Product
Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number: 72-RM50601,72-RM50602, 72-RM50603,72-RM50604 Product Description: Blue Nitrile Patient examination gloves
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3274-2026·2026-10-07
Alere San Diego Recalls hCG Urine Pregnancy Tests for False Positives
Alere San Diego is recalling multiple hCG urine pregnancy test models because they may detect low hCG levels, resulting in false positive results.
Product
Fisher Scientific Sure-Vue Urine hCG, Model/ Part: FHC-102/23900526; Henry Schein, Inc. One Step + Urine Cassette Test, Model/ Part: FHC-102/9004074, FHC-102/9004073; Alere hCG Cassette (25mIU/mL) in Urine, Model/ Part: FHC-102/92217; Cardinal Health hCG Cassette Rapid test…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3306-2026·2026-10-07
NOxBOXi Nitric Oxide Delivery System Recalled for Oxygen Sensor Defect
NOXBOX LTD is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems due to a manufacturing issue that may cause irregular oxygen readings.
Product
NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3320-2026·2026-10-07
Percussionaire In-Line Valve Recalled for Anesthetic Delivery Warning
Percussionaire Corporation is recalling 98,434 In-Line Valves to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Product
In-Line Valve, Product Number: P5-TEE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3303-2026·2026-10-07
Heraeus Medical Recalls PALACOS MV+G Pro Bone Cement Due to Leakage
Heraeus Medical is recalling PALACOS MV+G pro 40 and 80 bone cement due to potential monomer liquid leakage. The recall affects 20,523 units distributed worldwide.
Product
PALACOS MV+G pro 40; PALACOS MV+G pro 80. Model/Catalog Number: 5081290; 5081291. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3334-2026·2026-10-07
Wright Medical Recalls Charlotte Claw Screws Due to Missing Threads
Wright Medical Technology is recalling 34 Charlotte Claw Screws because missing threads on the screwheads may prevent secure engagement with the plate, potentially prolonging surgery.
Product
CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3290-2026·2026-10-07
FDA Recalls Defective Blue Nitrile Patient Examination Gloves
American Nitrile Operations LLC is recalling 36.8 million Opportunity Flex blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
Product
Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number: 72-50900, 72-50901, 72-50902, 72-50903, 72-50904 Product Description: Blue Nitrile Patient examination gloves
Category
Medical Device
Distribution
Distributed nationwide