State

Minnesota product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48251–48275 of 81668

ModerateFDA (Devices)·Z-1906-2017·2017-05-10
Breg Inc Recalls Unsealed Sterile Dressings for Cold Therapy Pads
Breg Inc is recalling approximately 2,609 sterile dressings used with cold therapy pads because some may have unsealed pouches, rendering them non-sterile.
Product
Dressing Shldr XL, P/N 04918 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1990-2017·2017-05-10
Anspach Effort Recalls Rotating Large Craniotomes Due to Missing Service Interval
The Anspach Effort, Inc. is recalling eight Rotating Large Craniotomes because the supplied directions for use did not include a recommended service interval.
Product
Rotating Large Craniotome
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1974-2017·2017-05-10
Anspach Effort Recalls 14CM Angle Attachment for Missing Service Interval
The Anspach Effort, Inc. is recalling 17 units of the 14CM Angle Attachment, Black Max because the supplied directions for use did not contain a recommended service interval.
Product
14CM ANGLE ATTACHMENT, BLACK MAX
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2033-2017·2017-05-10
Terumo Destination Renal Guiding Sheath Recalled for Missing Coating
Terumo Medical Corporation is recalling Destination Renal Guiding Sheaths because the distal end may lack the labeled 5 cm of coating, potentially making device navigation difficult.
Product
Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1891-2017·2017-05-10
Perouse Medical Recalls Dolphin Inflation Devices Due to Broken Blister
Perouse Medical is recalling 18,431 Dolphin Inflation Devices because of complaints regarding broken blisters. The devices were distributed in Arizona, Minnesota, and Tennessee.
Product
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND
Category
Medical Device
Distribution
3 states
ModerateFDA (Devices)·Z-2018-2017·2017-05-10
Anspach Effort 90 Degree Contra Angle Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 90 degree Contra Angle Attachments because the supplied directions for use did not contain a recommended service interval.
Product
90 degree Contra Angle Attachment Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1995-2017·2017-05-10
Anspach Effort Keyless Driver Pneumatic System Recall for Missing Service Interval
The Anspach Effort, Inc. is recalling 121 Keyless Driver pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Product
Keyless Driver Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0694-2017·2017-05-10
P & L Development Recalls Subpotent Diphenhydramine HCl Allergy Softgels
P & L Development is recalling 369,012 cartons of diphenhydramine HCl allergy softgels sold under multiple brands due to low potency test results.
Product
Allergy Relief Diphenhydramine HCl 25 mg, Antihistamine, Dye-Free, 24 Softgels, distributed under the following labels: (a) TopCare Allergy Relief, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, NDC 36800-483-24, UPC 0-36800-39134-5; (b) Rexall Since 1903…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2014-2017·2017-05-10
Anspach Effort 16cm Minimally Invasive Attachment Pneumatic System Recall
The Anspach Effort, Inc. is recalling 177 units of the 16cm Minimally Invasive Attachment because the supplied directions for use did not contain a recommended service interval.
Product
16cm Minimally Invasive Attachment Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1937-2017·2017-05-10
Anspach Effort Recalls Autolube-III Pneumatic Systems for Missing Service Interval
The Anspach Effort, Inc. is recalling 17 Autolube-III pneumatic systems because the supplied directions for use did not include a recommended service interval.
Product
Autolube-III with Foot Guard Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1999-2017·2017-05-10
Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 11.0cm Long Attachments for pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Product
11.0cm Long Attachment Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1916-2017·2017-05-10
Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Stability Issues
Smith & Nephew is recalling 2017 units of Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, THIN OSTEOTOME BLADE, 20 MM X 3 INCH, REF 71369220, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1938-2017·2017-05-10
Anspach Effort Recalls Autolube-III Pneumatic System for Missing Service Interval
The Anspach Effort, Inc. is recalling 51 units of the Autolube-III with Irrigation pneumatic system because the supplied directions for use did not contain a recommended service interval.
Product
Autolube-III with Irrigation Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2012-2017·2017-05-10
Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 8.0cm Medium Pneumatic System Attachments because the supplied directions for use did not contain a recommended service interval.
Product
8.0cm Medium Attachment Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1998-2017·2017-05-10
Anspach Effort IMRI Short HD Pneumatic Attachment Recall for Missing Service Interval
The Anspach Effort, Inc. is recalling five IMRI Short HD Pneumatic Attachments because the supplied directions for use did not include a recommended service interval.
Product
IMRI SHORT HD ATTACHMENT Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2009-2017·2017-05-10
Anspach Effort Minimal Access Attachment Pneumatic System Recall
The Anspach Effort, Inc. is recalling 618 Minimal Access Attachment pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Product
Minimal Access Attachment Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1986-2017·2017-05-10
Anspach Effort Adult Craniotome Pneumatic System Recall for Missing Service Interval
The Anspach Effort, Inc. is recalling Adult Craniotome Pneumatic Systems because the supplied Directions for Use did not contain a recommended service interval.
Product
Adult Craniotome Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1987-2017·2017-05-10
Anspach Effort 6.5cm Adult Cranial Thin Foot Plate Recall
The Anspach Effort, Inc. is recalling 130 units of 6.5cm Adult Cranial Thin Foot Plates because the supplied directions for use did not contain a recommended service interval.
Product
6.5CM ADLT CRANI, THIN FT PLATE Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0693-2017·2017-05-10
Amneal Recalls Rabeprazole Sodium Tablets for Failed Dissolution Specifications
Amneal Pharmaceuticals is recalling Rabeprazole Sodium Delayed Release Tablets, 20 mg, because the product failed to meet dissolution specifications.
Product
Rabeprazole Sodium Delayed Release Tablets, 20 mg, a) 30-count bottle (NDC 65162-0724-03), b) 90-count bottle (NDC 65162-0724-09), Rx Only, Manufactured by Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad INDIA 382220, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ 08807
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1915-2017·2017-05-10
Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Stability Data
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Product
RENOVATION, THIN OSTEOTOME BLADE, 12 MM X 3 INCH, REF 71369212, STERILE R, QTY: (1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1993-2017·2017-05-10
Anspach Compact Speed Reducer Recalled for Missing Service Interval Information
The Anspach Effort, Inc. is recalling 128 Compact Speed Reducer units because the supplied directions for use did not contain a recommended service interval.
Product
Compact Speed Reducer, 60:1 Black Max
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2016-2017·2017-05-10
Anspach Effort Recalls Otologic Curved Micro Pneumatic Systems
The Anspach Effort, Inc. is recalling 119 Otologic Curved Micro pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Product
Otologic Curved Micro Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0689-2017·2017-05-10
Fluconazole Tablets Recalled for Failed Dissolution Specifications
The Harvard Drug Group is recalling 914 cartons of Fluconazole 200 mg tablets because they failed to meet required dissolution specifications.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2002-2017·2017-05-10
Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 247 pneumatic system attachments because the supplied directions for use did not contain a recommended service interval.
Product
10.5cm Long Attachment Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2019-2017·2017-05-10
Anspach Effort Oscillating Micro-Saw Pneumatic System Recall
The Anspach Effort, Inc. is recalling 16 Oscillating MICRO-SAW pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Product
Oscillating MICRO-SAW Product Usage: Pneumatic system
Category
Medical Device
Distribution
Distributed nationwide