State

Wisconsin product recalls

72,936 recalls have nationwide distribution and so reach Wisconsin. 8,408 additional recalls listed Wisconsin specifically in their distribution scope.

What the numbers show

Total: 8,408
Critical: 1,547
Severe: 1,957
Most recent: 2026-09-09

Of the 8,408 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 1,957 (23%) are Severe.

Which agencies issued them

These figures cover only the 8,408 recalls whose distribution notice names Wisconsin specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3276–3300 of 81344

CriticalFDA (Devices)·Z-1324-2026·2026-02-18
Reprocessed ultrasound catheters recalled over residual material particles inside
Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.
Product
Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Bios
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1320-2026·2026-02-18
Reprocessed Inquiry catheters recalled over residual material particles inside
Medline is recalling 311 units because these lots of reprocessed catheters may contain small particles of residual material.
Product
Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1321-2026·2026-02-18
Reprocessed Livewire catheters recalled over residual material particles
Medline is recalling 41 reprocessed Livewire steerable diagnostic electrophysiology catheters because these lots may contain small particles of residual material.
Product
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH; Livewire Steerable Electrophysiology Cath
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1323-2026·2026-02-18
Reprocessed ViewFlex ICE catheters recalled over residual material particles
Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.
Product
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0353-2026·2026-02-18
UDENYCA syringes recalled after cartons were stored at room temperature
McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.
Product
UDENYCA — UDENYCA (PEGFILGRASTIM-CBQV)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1325-2026·2026-02-18
Reprocessed AcuNav catheters recalled over residual material particles inside
Medline is recalling 511 reprocessed Siemens ACUSON AcuNav diagnostic ultrasound catheters because these lots may contain small particles of residual material.
Product
Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1322-2026·2026-02-18
Reprocessed electrophysiology catheters recalled over residual material particles
Medline is recalling 48 reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters because these lots may contain small particles of residual material.
Product
Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 2-5-2mm 401211RH 401222RH 401223RH 401226RH 401227RH 401260RH 401261RH 401306RH 401309RH 401312RH 401430RH 40143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0322-2026·2026-02-18
Testosterone 87.5mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 62,581 pellets of Testosterone, 87.5 mg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone, 87.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1087-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0503-2026·2026-02-18
Peanut butter and grape jelly packs recalled over blue plastic
Ventura Foods is recalling 929 cases of 2.12oz packs after the firm found pieces of blue plastic in a filter during production.
Product
CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328
Category
Food
Distribution
40 states
HighFDA (Devices)·Z-1346-2026·2026-02-18
Azurion 7 B12 systems recalled over tables that may move unexpectedly
Philips is recalling 655 units of the Azurion 7 B12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1351-2026·2026-02-18
Azurion 5 M20 systems recalled over tables that may move unexpectedly
Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0330-2026·2026-02-18
Testosterone and triamcinolone pellets recalled over metal particulate matter
Asteria Health is recalling 1,631 pellets of Testosterone 87.5mg, Triamcinolone Acetonide 17.5 mcg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone 87.5mg, Triamcinolone Acetonide17.5 mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6087-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0313-2026·2026-02-18
Estradiol 22mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 133 pellets of ESTRADIOL, 22 mg sterile pellets over the potential presence of metal particulate matter.
Product
ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1339-2026·2026-02-18
GammaPlan 11.1 recalled over plans that may irradiate the wrong location
Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.
Product
Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1348-2026·2026-02-18
Azurion 7 M12 systems recalled over tables that may move unexpectedly
Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0326-2026·2026-02-18
Testosterone and anastrozole 4.5 pellets recalled over metal particulate matter
Asteria Health is recalling 100 pellets of Testosterone 100mg, Anastrozole 4mg (4.5) sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone 100mg, Anastrozole 4mg (4.5), 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0311-2026·2026-02-18
Estradiol 18mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 1,699 pellets of ESTRADIOL, 18 mg sterile pellets over the potential presence of metal particulate matter.
Product
ESTRADIOL, 18 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 3521, NDC: 79559-3018-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1349-2026·2026-02-18
Azurion 7 M20 systems recalled over tables that may move unexpectedly
Philips is recalling 5 of the Azurion 7 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1350-2026·2026-02-18
Azurion 5 M12 systems recalled over tables that may move unexpectedly
Philips is recalling 326 units of the Azurion 5 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1336-2026·2026-02-18
Circumcision trays recalled over open swabstick applicator seals
Medline is recalling 168 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1330-2026·2026-02-18
Vascular access kits and trays recalled over open swabstick seals
Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0323-2026·2026-02-18
Testosterone 100mg single pellets recalled over potential metal particulate
Asteria Health is recalling 153,498 pellets of Testosterone, 100 mg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone, 100 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC:79559-1100-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0317-2026·2026-02-18
Testosterone 18mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 146 pellets of Testosterone, 18.0 mg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone, 18.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1018-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0315-2026·2026-02-18
Estradiol 37.5mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 715 pellets of ESTRADIOL, 37.5 mg sterile pellets over the potential presence of metal particulate matter.
Product
ESTRADIOL, 37.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3037-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1335-2026·2026-02-18
Sterile resuture packs recalled over open swabstick applicator seals
Medline is recalling 216 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A
Category
Medical Device
Distribution
Distributed nationwide