State

Minnesota product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57101–57125 of 81684

SevereFDA (Drugs)·D-0227-2016·2015-11-18
The Compounder Recalls TRIEST 80/10/10 Capsules Due to Penicillin Contamination
The Compounder is recalling TRIEST 80/10/10 capsules because the active ingredient was contaminated with penicillin. Patients should stop using the medication and consult a healthcare provider.
Product
TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol USP (E3)) (23) 5MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0201-2016·2015-11-18
The Compounder Recalls BIEST TD 80/20 Cream Due to Penicillin Contamination
The Compounder is recalling BIEST TD 80/20 transdermal cream because an active ingredient was contaminated with penicillin. Patients should stop using the product and contact their healthcare provider.
Product
BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 6.5 : 30: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0182-2016·2015-11-18
The Compounder Recalls Biest 66/34 Due to Penicillin Cross-Contamination
The Compounder is recalling Biest 66/34 hormone suspension because an active ingredient was contaminated with penicillin. Patients should stop using the product and consult a healthcare provider.
Product
BIEST 66/34: TESTOSTERONE : PROGESTERONE IN OLIVE OIL(Estradiol USP Micronized (ED)/Estriol USP Micronized (E3): Testosterone : Progesterone in Olive Oil) 3mg : 4 mg : 100 mg/mL suspension, Rx only, packaged in a 15 mL glass dropper bottle. The Compounder, 340 Marshall Avenue…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0217-2016·2015-11-18
The Compounder Recalls Transdermal Cream Due to Penicillin Cross-Contamination
The Compounder is recalling specific lots of a compounded transdermal cream because an active ingredient was contaminated with penicillin.
Product
ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 35 : 0.5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0223-2016·2015-11-18
The Compounder Recalls Estriol Cream Due to Penicillin Cross-Contamination
The Compounder is recalling specific lots of Estriol transdermal cream because the active ingredient was contaminated with penicillin.
Product
ESTRIOL (E3) W/V (weight/volume) VERSABASE 3MG/ML Transdermal cream, dispensed in 5 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0226-2016·2015-11-18
The Compounder Recalls TRIEST 70/20/10 Transdermal Cream Due to Penicillin Contamination
The Compounder is recalling TRIEST 70/20/10 transdermal cream because the active ingredient was contaminated with penicillin. The recall covers 24 syringes per lot.
Product
TRIEST 70/20/10 ( Estriol USP / Estradiol USP (E2) / Estrone (E1) Triturate) [909] 12.5MG/ML transdermal cream, dispensed in 1 mL prefilled amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·15V765000·2015-11-18
Forest River Recalls Transit Buses with Defective Wheelchair Lifts
Forest River is recalling 2006-2014 Glaval buses equipped with specific Ricon wheelchair lifts due to a defect that could cause the platform to fall.
Product
GLAVAL BUS — GLAVAL BUS UNIVERSAL, TITAN II, TITAN, SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0254-2016·2015-11-18
GE Healthcare Recalls MRI Scanners Due to Potential SAR Limit Exceedance
GE Healthcare is recalling 756 MRI scanners because displayed SAR values may be lower than actual head SAR, potentially exceeding safety limits during head or neck scans.
Product
GE Healthcare, Discovery MR750w 3.0T. Product Usage: The Discovery MR750 3.0T, Discovery MR450 1.5T, Discovery MR750w 3.0T and the Optima MR450w 1.5T Systems are whole body magnetic resonance scanners for diagnostic imaging.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0255-2016·2015-11-18
GE Healthcare Recalls Signa 3.0T MRI Systems Due to SAR Display Error
GE Healthcare is recalling 19 Signa 3.0T MRI systems because displayed SAR values may be lower than actual head SAR, potentially exceeding safety limits.
Product
GE Healthcare, SIGNA 3.0T. Product Usage: Magnetic resonance system for diagnostic imaging. The indications for use for the 3.0T Signa VH/i (Signa 3.0T MR System) Transmit/Receive Body Imaging Coil expands the imaging capability of the 3.0T Signa VH/i MR Imaging System. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2016·2015-11-18
Teleflex Medical Recalls Rusch Flexi-slip Tracheal Tube Stylets
Teleflex Medical is recalling Rusch Flexi-slip tracheal tube stylets because the plastic coating may split or break off.
Product
Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0261-2016·2015-11-18
Stryker Vitallium Femoral Heads Recalled Due to Assembly Failure
Stryker Howmedica Osteonics Corp. is recalling 201 Vitallium femoral heads because they could not be assembled with their corresponding stems during surgery.
Product
Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0234-2016·2015-11-18
Miramar Labs Recalls miraDry System for Labeling Update on Lubricant Use
Miramar Labs is recalling 277 miraDry Systems to update labeling that reminds users to use only approved lubricants in a thin layer to prevent burns and blisters.
Product
miraDry System consisting of the MD4000-MC Console, the MD4000-HP miraDry Handpiece, and the MD4000-BT miraDry bioTip and accessories. General and Plastic Surgery: The miraDry System is intended for the treatment of primary axillary hyperhidrosis and was recently cleared for…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V767000·2015-11-18
Starcraft Prodigy and Quest School Buses Recalled for Wheelchair Lift Defect
Forest River is recalling 2006-2014 Starcraft Prodigy and Quest school buses equipped with specific Ricon wheelchair lifts due to a defect that could cause the platform to fall.
Product
STARCRAFT BUS — STARCRAFT BUS PRODIGY, QUEST
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0259-2016·2015-11-18
GE Healthcare Recalls Signa HDxt 3.0T MRI Scanners for SAR Limit Concerns
GE Healthcare is recalling 215 Signa HDxt 3.0T MRI scanners because displayed SAR values may be lower than actual head SAR, potentially exceeding safety limits.
Product
GE Healthcare, SIGNA HDxt 3.0T. Product Usage: The 1.5T Signa HDx family and 3.0T Signa HDx family are a whole body magnetic resonance scanner for use as a diagnostic imaging device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0243-2016·2015-11-18
Medtronic Recalls Amphirion Deep PTA Balloon Catheters Due to Seal Breach
Medtronic is recalling Amphirion Deep PTA Balloon Catheters because a potential breach in the pouch seal may compromise the sterilized product.
Product
Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152 AMP020150152 AMP025120152 AMP030080152 AMP040040152 AMP225210152 AMP020040152 AMP025040152 AMP025150152 AMP030120152 AMP040080152 AMP253210152 AMP020080152 AMP025080002 AMP030040002 AMP030150152…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0262-2016·2015-11-18
Philips HeartStart MRx Monitor/Defibrillator Recalled for Hardware Defects
Philips is recalling HeartStart MRx Monitor/Defibrillators because the CO2 inlet port can become inaccessible or the handle can separate from the housing.
Product
Philips HeartStart MRx Monitor/Defibrillator Models:M3535A, M3536A, M3536M, M3536MC, M3536M4, M3536M5 The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0264-2016·2015-11-18
Innokas Medical Recalls CARESCAPE VC150 Vital Signs Monitors for Shutdown Defect
Innokas Medical is recalling 424 CARESCAPE VC150 Vital Signs Monitors because the devices may shut down unintentionally without restarting.
Product
CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V766000·2015-11-18
Starcraft Transit Buses Recalled for Wheelchair Lift Bearing Defect
Forest River is recalling 2006-2014 Starcraft buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
Product
STARCRAFT BUS — STARCRAFT BUS ULTRASTAR, MVP, XLT, XPRESS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0213-2016·2015-11-18
The Compounder Recalls Hormone Capsules Due to Penicillin Cross-Contamination
The Compounder is recalling specific lots of compounded hormone capsules because an active ingredient was contaminated with penicillin.
Product
E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized (E3) : PROGEST (Progesterone USP Micronized) : TESTOST (Testosterone USP) IN OLIVE OIL 0.75 : 3 : 50 : 5MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0242-2016·2015-11-18
WalkMed Infusion Pumps Recalled for Air Detection Failure
WalkMed Infusion is recalling Triton Infusion Pumps because they may fail to detect air in the line when infusing Venofer.
Product
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump). Used to pump fluids into a patient in a controlled manner.
Category
Medical Device
Distribution
22 states
HighFDA (Devices)·Z-0241-2016·2015-11-18
DeRoyal Surgical Kits Recalled Due to Sterilant Exposure
DeRoyal Industries is recalling specific lots of sterile surgical kits containing 3M DuraPrep solution due to unintended exposure to sterilant during the sterilization process.
Product
DeRoyal Sterile Custom Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical Solution, Catalog No. 8630, Lot Nos: 2016-09EE or 2016-09EF, or 2016-09EG, or Catalog No. 863, Lot No. 2016-08DC: TOTAL JOINT PACK A&B, REF 89-5720.04; PACEMAKER PACK, REF 89-6717.03
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0250-2016·2015-11-18
Ceterix NovoCut Suture Manager Recalled for Suture Cutting Risk
Ceterix Orthopedics is recalling 1,364 NovoCut Suture Manager devices because they may cut sutures during knot tensioning, causing knots to unravel.
Product
NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0256-2016·2015-11-18
GE Healthcare Recalls SIGNA Excite 3.0T MR Systems for SAR Display Error
GE Healthcare is recalling 55 SIGNA Excite 3.0T MR systems because displayed SAR values may be lower than actual head SAR levels during scans.
Product
GE Healthcare, SIGNA Excite 3.0T. MR System for use as a diagnostic imaging device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0236-2016·2015-11-18
Synthes Recalls Small Notch Titanium Reconstructive Plate Sets
Synthes is recalling Small Notch Titanium Reconstructive Plate sets because they are being used in spine surgeries, which is a contraindicated use for these trauma products.
Product
Synthes Small Notch Titanium Reconstructive Plate set (SNTRP). Ti PLATE/ROD/PLATE 231mm 6HOLES/5.0mm ROD/17HOLES. Orthopedic implant.
Category
Medical Device
Distribution
18 states
HighNHTSA·15V769000·2015-11-18
Micro Bird School Bus Recall for Wheelchair Lift Bearing Defect
Micro Bird is recalling 2006-2014 school buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
Product
MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, T-SERIES SCHOOL BUS, MB II SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide