State

Wisconsin product recalls

72,820 recalls have nationwide distribution and so reach Wisconsin. 8,407 additional recalls listed Wisconsin specifically in their distribution scope.

What the numbers show

Total: 8,407
Critical: 1,547
Severe: 1,956
Most recent: 2026-09-02

Of the 8,407 recalls naming Wisconsin we have scored against our rubric, 1,547 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,956 (23%) are Severe.

Which agencies issued them

These figures cover only the 8,407 recalls whose distribution notice names Wisconsin specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

76–100 of 81227

HighFDA (Devices)·Z-2994-2026·2026-09-02
Medline Medical Convenience Kits Recalled for Endotoxin Levels
Medline Industries is recalling 2,262 medical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Product
Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit SKU DYNJ40154D; 3) ENT PACK, Medline Kit SKU DYNJ40154F; 4) ENT SCOPE PACK, Medline Kit SKU DYNJ44480D; 5) ENT NASAL ORAL PACK MOSES, Medline Kit SKU
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3032-2026·2026-09-02
Healthmark Protein Test Recalled Due to Expired Ingredient
Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Product
healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3021-2026·2026-09-02
Medline Head and Neck Kits Recalled for Contaminated Component
Medline is recalling 24 convenience kits labeled as MAJOR HEAD AND NECK PPS because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS, Medline Kit SKU DYNJ9425991S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1277-2026·2026-09-02
Byron White Herbal Supplement Recalled for Undeclared Walnut Allergen
Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.
Product
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-3033-2026·2026-09-02
IMRIS ORT200 Operating Room Table Recalled for Mechanical Failure Risk
IMRIS Imaging Inc is recalling six ORT200 operating room tables because a mechanical failure could cause unintended movement and patient injury.
Product
ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2988-2026·2026-09-02
Philips Incisive CT Recalled for Potential Failure to Trigger Clinical Scan
Philips is recalling Incisive CT scanners with specific software versions due to a potential failure to trigger clinical scans during bolus tracking.
Product
Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3024-2026·2026-09-02
Medline Recalls 663 Surgical Convenience Kits Due to Contamination
Medline Industries is recalling 663 surgical convenience kits distributed nationwide because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: 1) MAJOR GYN PACK, Medline Kit SKU DYNJG001030C; 2) GYN LITHOTOMY PACK, Medline Kit SKU DYNJT8166; 3) OPEN HEART PACK, Medline Kit SKU DYNJ47638B; 4) EAST DAVINCI, Medline Kit SKU DYNJ900949C; 5) THORACIC, Medline Kit SKU DYNJ903470
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1276-2026·2026-09-02
Byron White A-L Complex Herbal Supplement Recalled for Undeclared Walnut
Byron White Formulas is recalling A-L Complex Herbal Supplement because the label does not declare walnuts in English, posing a risk to individuals with nut allergies.
Product
Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-3013-2026·2026-09-02
Midmark Digital ECG Software Recall for Incorrect Waveform Display
Midmark is recalling Digital ECG HD+12 and HD+15 units with specific IQecg plugin software versions due to a communication anomaly that may cause incorrect ECG waveforms and inaccurate heart rate calculations.
Product
Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0781-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 125 mcg tablets because they are subpotent. The recall is ongoing nationwide.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2998-2026·2026-09-02
Hollister Recalls Onli Hydrophilic Urethral Catheters Due to Manufacturing Defect
Hollister is recalling specific lots of Onli hydrophilic urethral intermittent catheters because a manufacturing defect may cause a protrusion that leads to genitourinary trauma or bleeding.
Product
Onli 17cm Hydrophilic Urethral Intermittent Catheter, labeled as: 1) 82081 Ch08-17 Onli Hydrophilic Urethral Intermittent Catheter, SKU/REF 82081; 2) 82101 Ch10-17 Onli Hydrophilic Urethral Intermittent Catheter, SKU/REF 82101; 3) 82121 Ch12-17 Onli Hydrophilic Urethral In
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3022-2026·2026-09-02
Medline recalls surgical convenience kits due to potential contamination
Medline Industries is recalling 94 surgical convenience kits nationwide because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY, Medline Kit SKU DYNJ903479L; 4) LAPAROSCOPY, Medline Kit SKU DYNJ903479M.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3019-2026·2026-09-02
Medline Recalls 71 Convenience Kits Due to Contaminated Component
Medline Industries is recalling 71 FEMORAL PACK and FEVAR convenience kits because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: 1) FEMORAL PACK, Medline Kit SKU DYNJ909393A; 2) FEVAR, Medline Kit SKU DYNJ910295D.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3020-2026·2026-09-02
Medline Recalls 263 Surgical Convenience Kits Due to Contamination
Medline Industries is recalling 263 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide in 18 states.
Product
Medline convenience kits labeled as: 1) OPEN HEART PACK, Medline Kit SKU CDS840393P; 2) OPEN HEART PACK, Medline Kit SKU CDS840393Q; 3) OPEN HEART PROCEDURE, Medline Kit SKU CDS980895W; 4) VALVE CDS, Medline Kit SKU CDS981551G; 5) FEM POP, Medline Kit SKU CDS982028W;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2995-2026·2026-09-02
Medline Medical Convenience Kits Recalled for Endotoxin Levels
Medline is recalling 246 surgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Product
Medline medical convenience kits, labeled as: 1) CRANIOTOMY PACK, Medline Kit SKU DYNJT6545; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ88056A; 3) ENT SINUS PACK, Medline Kit SKU DYNJ89001; 4) THYROID ENT, Medline Kit SKU DYNJ908641.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3009-2026·2026-09-02
AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
AVID Medical is recalling 120 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Product
Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0789-2026·2026-09-02
Lupin Recalls Clobetasol Propionate Cream for Content Uniformity Failures
Lupin Pharmaceuticals is recalling Clobetasol Propionate Cream 0.05% because it failed content uniformity specifications. The recall covers 5,082 tubes distributed nationwide.
Product
CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3007-2026·2026-09-02
AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Error
AVID Medical, Inc. is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Product
Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2999-2026·2026-09-02
Medline Trach Tube Kit Recalled for Component Labeling Discrepancy
Medline is recalling 45 Trach Tube Kits (SKU DYKM2330) due to a component labeling discrepancy. The recall covers units distributed in California.
Product
Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3016-2026·2026-09-02
Henry Schein Recalls Dental Composite Capsules Due to Incorrect Packaging
Henry Schein Inc. is recalling specific lots of Grandio Universal Nano-Hybrid Restorative Material capsules because they were distributed with incorrect packaging and Instructions for Use.
Product
Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594, Mfr Product Code 1840; Lots 2529604, 2538147, 2608145 2) 949-3595, Mfr Product Code 1841; Lots 2539075, 2539313, 2609789, 2539065 3) 949-3596, Mfr Product Code 1842; Lots 253663
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3006-2026·2026-09-02
AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Product
Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3035-2026·2026-09-02
Olympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.
Product
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3000-2026·2026-09-02
American Contract System Convenience Kit Recalled for Performance Failures
American Contract Systems Inc is recalling 30 units of Convenience Kits containing Medline catheters because samples failed performance specifications.
Product
American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3010-2026·2026-09-02
AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
AVID Medical, Inc. is recalling 130 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Product
Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3018-2026·2026-09-02
ConMed Suture Anchor Recalled for Incorrect Patient Implant Card
ConMed is recalling specific suture anchors because they may contain incorrect patient implant cards, which could lead to incorrect device identification and traceability.
Product
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile
Category
Medical Device
Distribution
Distributed nationwide