State

Wisconsin product recalls

73,584 recalls have nationwide distribution and so reach Wisconsin. 8,448 additional recalls listed Wisconsin specifically in their distribution scope.

What the numbers show

Total: 8,448
Critical: 1,562
Severe: 2,304
Most recent: 2026-10-24

Of the 8,448 recalls naming Wisconsin we have scored against our rubric, 1,562 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,304 (27%) are Severe.

Which agencies issued them

These figures cover only the 8,448 recalls whose distribution notice names Wisconsin specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22976–23000 of 82032

HighFDA (Devices)·Z-1021-2022·2022-05-11
In Vitro Diagnostic Estradiol Test Recalled for Falsely Elevated Results
Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol (eE2) 500T diagnostic kits that produce falsely elevated test results in plasma specimens, which could lead clinicians to misinterpret patient results.
Product
Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0838-2022·2022-05-11
Losartan Potassium tablets recalled for AZIDO impurity above limits
Lupin Pharmaceuticals recalls Losartan Potassium tablets for CGMP deviations with AZIDO impurity above limits. The recall affects 657,336 bottles distributed nationwide; no illnesses reported.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V323000·2022-05-11
Nova Bus Recalls LFS and LFS Artic Buses Due to Signal Confusion
Nova Bus is recalling 2016-2020 LFS and 2013-2022 LFS Artic buses because a text message board duplicates stop and turn signals, increasing crash risk.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1029-2022·2022-05-11
Robotic-Assisted Medical Device Recalled Due to Software Defect
The FDA is recalling the VELYS Robotic-Assisted Solution Base due to a software defect in version 1.5.1 related to Daylight Saving Time changes. The defect can cause system errors requiring restart, potentially delaying patient treatment.
Product
VELYS Robotic-Assisted Solution Base Product No.: 451570100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1024-2022·2022-05-11
Siemens ADVIA Centaur Estradiol Test Recalled for Falsely Elevated Results
Siemens Healthcare is recalling all lots of the ADVIA Centaur Enhanced Estradiol diagnostic test because plasma specimens can produce falsely elevated results, potentially leading clinicians to misinterpret patient results.
Product
ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1020-2022·2022-05-11
Estradiol diagnostic test kits recalled for falsely elevated results
Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.
Product
Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1025-2022·2022-05-11
Estradiol Diagnostic Device Recalled for Falsely Elevated Test Results
An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.
Product
ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0834-2022·2022-05-11
Losartan Potassium Tablets Recalled for Excessive Azido Impurity
Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1037-2022·2022-05-11
Elegant Foods Mint Macaron Recall for Undeclared Food Colorings
Elegant Foods is recalling Mint Macaron products due to missing label declarations for six artificial food colorings. Consumers should stop consumption and return affected products.
Product
elegant foods Mint Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1034-2022·2022-05-11
Elegant Foods Eggnog Macaron Cases Recalled for Undeclared Food Colors
Elegant Foods is recalling eggnog macaron cases because the packaging fails to disclose food color additives including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.
Product
elegant foods Eggnog Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-0831-2022·2022-05-11
Drug recall: Vancomycin HCl injection bags for manufacturing deviations
SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.
Product
Vancomycin HCl 1.5 g in 0.9% Sodium Chloride, 500 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0924-44
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0851-2022·2022-05-11
Erythromycin Topical Gel Recalled Due to Manufacturing Quality Deviations
McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.
Product
Erythromycin Topical Gel USP, 2%, Net Wt 60 g tube, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-053-68
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0846-2022·2022-05-11
Lidocaine Oral Topical Solution Recalled Due to Failed Viscosity Specification
Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.
Product
Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701, NDC 50383-775-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1026-2022·2022-05-11
Cervical Cage Trial Kit Recalled for Incorrect Size Labeling
restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.
Product
Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1032-2022·2022-05-11
Elegant Foods Lemon Macarons Recalled for Undeclared Food Color Additives
Elegant Foods is recalling Lemon Macarons (Code 213645A) because the product contains six food color additives that are not declared on the packaging.
Product
elegant foods Lemon Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1040-2022·2022-05-11
Elegant Foods Macarons Recalled for Undeclared Food Coloring
Elegant Foods is recalling macarons due to missing declarations of six synthetic food colors on the packaging. Consumers sensitive to food dyes should not consume this product.
Product
elegant foods Macaron Variety A, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1041-2022·2022-05-11
Elegant Foods Macarons Recalled for Undeclared Food Colorants
Elegant Foods, LLC is recalling Macaron Variety B due to undeclared food colorants on the label. The product contains six FD&C dyes not listed in the ingredient declaration.
Product
elegant foods Macaron Variety B, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-0829-2022·2022-05-11
Norepinephrine Injection Recalled Nationwide for Manufacturing Quality Deviations
SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.
Product
Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-078-40
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1035-2022·2022-05-11
Elegant Foods Fall Spice Macarons Recalled for Undeclared Food Coloring
Elegant Foods is recalling Fall Spice Macarons because the packaging does not declare six artificial food colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.
Product
elegant foods Fall Spice Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1042-2022·2022-05-11
Holiday Macaron Variety Recalled for Undeclared Food Colors
Elegant Foods is recalling Holiday Macaron Variety packages due to missing label declarations for six FDA-approved food colorants. Consumers with sensitivities to dyes should not consume these products.
Product
elegant foods Holiday Macaron Variety, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1036-2022·2022-05-11
Elegant Foods Lavender Macaron Recall for Undeclared Food Colors
Elegant Foods is recalling Lavender Macarons (code 21264A) due to undeclared food colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40. Affected cases were distributed in Wisconsin.
Product
elegant foods Lavender Macaron, Case of 100. 537 Atlas Ave, Madison, WI 53714.
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-0842-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Impurity
Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide Tablets Recalled Due to AZIDO Impurity Contamination
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2022·2022-05-11
Drug recall: fentanyl and bupivacaine injectable solution manufacturing deviations
SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.
Product
Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0231-32
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V320000·2022-05-10
Land Rover Recalls 2022 New Range Rovers for Front Crash Sensor Defect
Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.
Product
LAND ROVER — LAND ROVER NEW RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide