State

Minnesota product recalls

73,824 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,851
Critical: 1,137
Severe: 2,246
Most recent: 2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51851–51875 of 81675

ModerateFDA (Devices)·Z-0033-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color C4 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 10 units of Zenostar MT Color C4 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color C4 60ml, art. no. 681062. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0023-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color A3 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 42 units of Zenostar MT Color A3 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color A3 60ml, art. no. 681052. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0034-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color D2 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 40 units of Zenostar MT Color D2 dental porcelain coloring liquid due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color D2 60ml, art. no. 681063. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0022-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color A2 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling Zenostar MT Color A2 dental porcelain coloring liquid because packaging leaks may cause skin irritation.
Product
Zenostar MT Color A2 60ml, art. no. 681051. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0021-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color A1 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling Zenostar MT Color A1 dental porcelain coloring liquid because packaging leaks may cause skin irritation.
Product
Zenostar MT Color A1 60ml, art. no. 681050, Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0030-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color C1 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 37 units of Zenostar MT Color C1 dental porcelain coloring liquid because packaging leaks may cause skin irritation.
Product
Zenostar MT Color C1 60ml, art. no. 681059. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2907-2016·2016-10-12
Integra Lumbar Drainage Set Recalled for Incomplete Packaging Seal
Integra LifeSciences is recalling 18 units of Integral Lumbar Drainage Sets due to incomplete sterile packaging seals discovered during final inspection.
Product
Integral Lumbar Drainage Set, REF 910420, Sterile EO, Rx only, primary packaged in a PVC blister sealed with Tyvek sheet and secondary packaged in to Tyvek pouch. Internal drainage set is primary packaged in a Tyvek pouch and secondary packaged in to Tyvek pouch, One (1) sealed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0010-2017·2016-10-12
Philips CT Scanner Recall for Infant Head Image Quality Defects
Philips is recalling 358 Ingenuity Core CT scanners because infant head scans may show degraded image quality, including non-uniformity and CT number shifts.
Product
Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0011-2017·2016-10-12
Philips Ingenuity Core 128 CT Scanner Recalled for Image Quality Defects
Philips Medical Systems is recalling 524 Ingenuity Core 128 CT scanners because high-resolution head scans may produce degraded image quality, including non-uniformity and CT number shifts.
Product
Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0046-2017·2016-10-12
Toshiba Aquilion Lightning CT Scanner Recalled for Reconstruction Error
Toshiba is recalling 165 Aquilion Lightning CT scanners because a reconstruction error may interrupt scanning if the scan range exceeds the maximum Field of View.
Product
Toshiba America Medical Systems, Inc Aquilion Lightning TSX-035A CT Scanner.
Category
Medical Device
Distribution
35 states
ModerateFDA (Devices)·Z-2910-2016·2016-10-12
Integra Lumbar Drainage Set Recalled Due to Incomplete Packaging Seal
Integra LifeSciences Corp. is recalling specific lots of Lumbar Drainage Sets because final inspection revealed an incomplete packaging seal on the sterile product.
Product
Integra Lumbar Drainage Set, REF 910120A, Sterile EO, Rx only, primary packaged in a PVC blister sealed with Tyvek sheet and secondary packaged in to Tyvek pouch. External drainag system is primary packaged in a Tyvek pouch and secondary packaged in to Tyvek pouch. One (1)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0037-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color Impulse Orange Dental Porcelain
Ivoclar Vivadent is recalling 5 units of Zenostar MT Color Impulse orange dental porcelain due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color Impulse orange, art. no. 681168. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0031-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color C2 Dental Porcelain Coloring Liquid
Ivoclar Vivadent is recalling 19 units of Zenostar MT Color C2 dental porcelain coloring liquid due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color C2 60ml art. no. 681060. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0029-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color B4 Dental Porcelain Liquid
Ivoclar Vivadent is recalling 7 units of Zenostar MT Color B4 dental porcelain liquid due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color B4 60ml, art. no. 681058. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2911-2016·2016-10-12
Arrow Recalls Walrus Arterial Embolectomy Catheters Due to Labeling Errors
Arrow International Inc is recalling 2,425 Walrus Arterial Embolectomy Catheters nationwide due to incorrect labeling.
Product
Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0020-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color Impulse Violet Due to Packaging Leaks
Ivoclar Vivadent is recalling 25 units of Zenostar MT Color Impulse violet dental porcelain coloring due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color Impulse violet, art. no. 681166 Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0025-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color A4 Dental Porcelain Liquid
Ivoclar Vivadent is recalling 11 units of Zenostar MT Color A4 dental porcelain liquid due to potential packaging leaks that may cause skin irritation.
Product
Zenostar MT Color A4 60ml, art. no. 681054. Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0007-2017·2016-10-12
Sun Pharmaceutical Recalls Bupropion Hydrochloride Tablets for Dissolution Failures
Sun Pharmaceutical Industries is recalling 31,762 bottles of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0009-2017·2016-10-12
Philips Brilliance 64 CT Scanner Recalled for Infant Head Image Quality Issues
Philips Medical Systems is recalling 185 Brilliance 64 CT scanners because infant head scans in High Resolution mode may show degraded image quality.
Product
Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0019-2017·2016-10-12
Ivoclar Vivadent Recalls Zenostar MT Color Impulse Grey Dental Porcelain
Ivoclar Vivadent is recalling 60 units of Zenostar MT Color Impulse grey dental porcelain due to packaging leaks that may cause skin irritation.
Product
Zenostar MT Color Impulse grey, art. no. 681167 Product Usage: For coloring dental porcelain
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0001-2017·2016-10-12
Varithena Administration Packs Recalled Due to Incorrect Syringe Type
Biocompatibles is recalling Varithena administration packs because they contain the incorrect type of syringe. The recall covers 3,254 packs distributed nationwide.
Product
VARITHENA — VARITHENA (POLIDOCANOL)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0001-2017·2016-10-12
Terumo CDI H/S Cuvette Recall Due to Connection Error
Terumo is recalling CDI H/S Cuvettes because they may fail to connect to the probe, causing the monitor to display an error and preventing blood parameter display.
Product
CDI¿ H/S Cuvette The intended use for the CDI¿ H IS Cuvette is as follows: The CDI¿ H/S Cuvettes are intended for use with a CDI monitor during cardiopulmonary bypass procedures when continuous monitoring of blood hematocrit and oxygen saturation is desired.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2912-2016·2016-10-12
Siemens RAPIDPoint 400 Cartridges Recalled for Chloride Calibration Error
Siemens is recalling RAPIDPoint 400 Measurement Cartridges because of an error in the value assignment for Chloride calibrators.
Product
Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756, 10341161
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2913-2016·2016-10-12
Siemens RAPIDPoint 405 Cartridges Recalled for Chloride Calibration Error
Siemens Healthcare Diagnostics is recalling RAPIDPoint 405 Measurement Cartridges due to an error in the value assignment for Chloride calibrators.
Product
Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812, 1028322, 10313971 , 10310469
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0006-2017·2016-10-12
Shire Recalls Vyvanse Capsules Due to Presence of Foreign Tablets
Shire is recalling 7,680 bottles of Vyvanse 30 mg capsules because foreign tablets or capsules were found in the product.
Product
VYVANSE — VYVANSE (LISDEXAMFETAMINE DIMESYLATE)
Category
Drug
Distribution
Distributed nationwide