State

Minnesota product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53626–53650 of 81678

HighFDA (Devices)·Z-2104-2016·2016-07-06
Medical Depot Recalls Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail and detach from the ground.
Product
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16208·2016-07-06
PTX Performance Products Recalls Airwalk Hoverboards Due to Fire Hazard
PTX Performance Products is recalling about 4,900 Airwalk self-balancing scooters because the lithium-ion batteries can overheat, posing a risk of fire or explosion.
Product
Self-balancing scooters/hoverboards
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2062-2016·2016-07-06
Hospira Recalls LifeShield IV Sets Due to Potential Fluid Leakage
Hospira is recalling approximately 3.9 million LifeShield IV administration sets because fluid may leak at the secondary port.
Product
*** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML BURETTE PLUMSET, CONVERTIBLE PIN, CLAVE SECONDARY PORT, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 118 IN; PRIMING VOLUME: 14 ML; *** 2) Product labeled in part: List No. 19685-28…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16209·2016-07-06
Yuka Clothing Recalls Self-Balancing Scooters Due to Fire Hazard
Yuka Clothing is recalling about 800 self-balancing scooters sold nationwide and online because the lithium-ion battery packs can overheat, posing a risk of smoking, fire, or explosion.
Product
Self-balancing scooters/hoverboards
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2054-2016·2016-07-06
Nephron Recalls Sodium Chloride Inhalation Solution Due to Sterility Concerns
Nephron Pharmaceuticals is recalling 13,692 cartons of Sodium Chloride Inhalation Solution due to a failure in the internal dye ingress test, which raises concerns about the sterility of the vials.
Product
Sodium Chloride Inhalation Solution, USP 7%, 60 x 4 mL Sterile Unit-Dose Vials, Rx Only, NDC 0487-9007-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is indicated. For…
Category
Medical Device
Distribution
36 states
HighFDA (Devices)·Z-2049-2016·2016-07-06
Baxter Recalls PrismaSate Dialysis Solution Bags Due to Leaks
Baxter Healthcare is recalling 10,054 units of PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy because of leaks near the top of the bags.
Product
PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy
Category
Medical Device
Distribution
32 states
HighCPSC·16756·2016-07-06
Little Lotus Baby Swaddles and Sleeping Bags Recalled for Choking Hazard
Embrace Technologies is recalling Little Lotus baby swaddles and sleeping bags because shoulder snaps can break or detach, posing a choking hazard to young children.
Product
Little Lotus baby swaddles and sleeping bags
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2087-2016·2016-07-06
Siemens Hettich Centrifuge Modules Recalled for Premature Bucket Failures
Siemens Healthcare Diagnostics Inc. is recalling 487 Hettich Centrifuge Modules due to premature bucket failures. The units were distributed nationwide.
Product
Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module (10703032 or 10713761) FlexLab High Throughput Centrifuge Module (11171747) FlexLab and Aptio Centrifuge Module (10628157 or 11266581): Used to separate…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2105-2016·2016-07-06
Medical Depot Recalls Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail.
Product
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2103-2016·2016-07-06
Medical Depot Universal Aluminum Crutches Recalled for Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Universal aluminum crutches because the bottom metal tips may fail.
Product
Universal aluminum crutch, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2102-2016·2016-07-06
Medical Depot Recalls EZ Adjust Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of EZ adjust aluminum crutches because the tip may fail, posing a risk of injury.
Product
EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V510000·2016-07-06
MCI Recalls 2015-2016 J4500 Buses Due to Window Hardware Defect
Motor Coach Industries is recalling 2015-2016 J4500 buses because improperly installed window hardware may allow windows to open unexpectedly, increasing ejection risk.
Product
MCI — MCI J4500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2059-2016·2016-07-06
Hospira Recalls LifeShield IV Administration Sets Due to Fluid Leakage
Hospira is recalling specific LifeShield IV administration sets because intravenous fluid may leak at the CLAVE secondary port.
Product
*** 1) Product labeled in part: 14951-48; LIFESHIELD; PLUMSET WITH CONVERTIBLE PIERCING PIN, TWO INTEGRAL CLAVE PORTS AND CLAVE ON SECONDARY PORT; NOMINAL LENGTH: 104 IN (264 CM); PRIMING VOLUME: 19 ML; *** 2) Product labeled in part: 14952-01; LIFESHIELD; HEMA Y-TYPE BLOOD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2061-2016·2016-07-06
Hospira Recalls IV Administration Sets Due to Fluid Leakage Risk
Hospira is recalling specific lots of Lifeshield IV administration sets because intravenous fluid may leak at the secondary port.
Product
*** 1) Product labeled in part: 19734-28; LIFESHIELD; LIFESHIELD LATEX-FREE PLUM SET, MICRODRIP,PP SOLUSET,FILTER, 3 CLAVE PORTS, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 124 IN (315 IN); PRIMING VOLUME: 14 ML; *** 2) Product labeled in part: 19732-28; LIFESHIELD; LIFESHIELD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2093-2016·2016-07-06
Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect
Smith & Nephew is recalling 16 units of the Legion HK Femoral Assembly because the internal surface where cement is applied is below specification.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 4 RIGHT, A/P 58.5 MM, M/L 66 MM, REF 71421364 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2058-2016·2016-07-06
Hospira Recalls PlumSet IV Administration Sets Due to Fluid Leakage
Hospira is recalling specific PlumSet IV administration sets because intravenous fluid may leak at the CLAVE secondary port.
Product
*** 1) Product labeled in part: List No. 14212-28; LIFESHIELD; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-DEHP; *** 2) Product labeled in part: List No. 14254-28; LIFESHIELD; PRIMARY PLUMSET; CLAVE Port 2 CLAVE Y-Sites, 0.2 Micron Filter, 112…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2101-2016·2016-07-06
Medical Depot Recalls Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of aluminum crutches nationwide because the metal tip may fail. Users should stop using the product.
Product
Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, adult, 8 pairs per case, 3) Aluminum crutch, youth, 1 pair per case, 4) Aluminum crutch 8 pairs per case, 5) Aluminum crutch, tall adult, 1 pair per case & 6) Aluminum…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2106-2016·2016-07-06
Medical Depot Aluminum Crutches Recalled Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Direct Supply aluminum crutches because the metal tips may fail.
Product
Direct Supply aluminum crutch, adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16212·2016-07-06
Boscov's Recalls Orbit Hoverboards Due to Fire and Explosion Hazard
Boscov's is recalling Orbit brand self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of fire or explosion.
Product
Self-balancing scooters/hoverboards
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2098-2016·2016-07-06
CMP Industries Recalls Impak Elastic Acrylic Resin Due to Rust
CMP Industries is recalling Impak Elastic Acrylic Resin Powder and Liquid due to the possible presence of foreign material, specifically rust.
Product
IMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID, SHADE TRANSPARENT, CONTENTS: 454 gm Powder + 325ml Liquid, REF 3746, Rx ONLY; Indicated for relining a denture surface
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-2055-2016·2016-07-06
Hospira Symbiq Infusion Pumps Recalled for Frequent False Occlusion Alarms
Hospira is recalling Symbiq One Channel Infusers due to frequent false proximal occlusion alarms that may delay or interrupt patient therapy.
Product
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2063-2016·2016-07-06
Medtest Homocysteine Reagent Recalled for Performance Deterioration
Medtest Holdings is recalling 13 kits of Liquid Stable 2-Part Homocysteine Reagent due to under-recovery of homocysteine in patient samples.
Product
Liquid stable 2 part Homocysteine Reagent, for in vitro quantitative determination of total homocysteine in human serum and plasma - H7575-57 kit includes one Rl and one R2 bottle and one bottle of calibrator level 1 and one bottle of calibrator level 2.
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-2090-2016·2016-07-06
Smith & Nephew Recalls Legion HK Femoral Assemblies for Surface Defect
Smith & Nephew is recalling 12 units of Legion HK Femoral Assemblies because the internal surface is below specification, potentially affecting cement adhesion.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 3 LEFT, A/P 54.5 MM, M/L 62 MM, REF 71421373 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2097-2016·2016-07-06
CMP Industries Recalls IMPAK Liquid Acrylic Resin Due to Rust
CMP Industries is recalling 77 units of IMPAK Liquid Acrylic Resin due to the possible presence of foreign material (rust). The affected product is distributed in six US states and Canada.
Product
IMPAK Liquid Acrylic Resin sold under the following labels: 1) IMPAK ELASTIC ACRYLIC RESIN LIQUID FOR MOUTHGUARDS & BRUXISM SPLINTS, Contents: 1 Quart (946 ML), REF 3306, Rx ONLY; 2) IMPAK ELASTIC ACRYLIC RESIN LIQUID FOR MOUTHGUARDS & BRUXISM SPLINTS, Contents: 11 oz (325 ML)…
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2094-2016·2016-07-06
Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect
Smith & Nephew is recalling 10 units of Legion HK Femoral Assemblies because the internal cement surface is below specification.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 5 LEFT, A/P 62 MM, M/L 70 MM, REF 71421375 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide