State

Minnesota product recalls

73,722 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,849
Critical: 1,137
Severe: 2,245
Most recent: 2026-10-28

Of the 7,849 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 2,245 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30376–30400 of 81571

HighFDA (Devices)·Z-2955-2020·2020-09-23
Integra Padgett Electric Dermatome Set Recalled Due to Cable Melting
Integra LifeSciences is recalling 2 units of the Padgett Electric Dermatome Set because the handpiece cable melts after sterilization.
Product
Integra Padgett Electric Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2963-2020·2020-09-23
Randox Lactate Dehydrogenase Reagent Recall for Carryover Avoidance
Randox Laboratories is recalling Lactate Dehydrogenase P-L reagent to address reagent carryover issues on RX instruments that may cause erroneous test results.
Product
Lactate Dehydrognease P-L, (UV), Catalog Number LD3818 - Product Usage: device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum and plasma. This product is suitable for use on the RX series instruments which includes the RX…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1599-2020·2020-09-23
RLC Labs Recalls Nature-Throid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling Nature-Throid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The product was manufactured under conditions found to be subpotent.
Product
Nature-Throid, Thyroid USP [liothyronine (T3) 11.25 mcg and levothyroxine (T4) 47.5 mcg], 1.25 Grain (81.25 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3303-4; b) 60-count bottles, NDC 64727-3303-5; c) 90-count bottles, NDC 64727-3303-6; d) 100-count bottles, NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2981-2020·2020-09-23
Roche Recalls Anti-TPO Assay Kits Due to Updated Interference Claim
Roche Diagnostics is recalling 11,870 Elecsys Anti-TPO Assay kits because internal studies found the radio frequency interference claim no longer met for specific cobas e analyzers.
Product
Elecsys Anti-TPO Assay on cobas e analyzers 411, 601, 602, Catalog Number 06368590190
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1598-2020·2020-09-23
RLC Labs Recalls Nature-Throid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling Nature-Throid tablets due to manufacturing deviations. The products were manufactured under conditions found to be subpotent.
Product
Nature-Throid, Thyroid USP [liothyronine (T3) 4.5 mcg and levothyroxine (T4) 19 mcg], 1/2 Grain (32.5 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3299-4; b) 60-count bottles, NDC 64727-3299-5; c) 90-count bottles, NDC 64727-3299-6; d) 100-count bottles, NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2967-2020·2020-09-23
Tosoh Bioscience Recalls AIA-PACK HCG Calibrator Sets Due to Stability Issues
Tosoh Bioscience is recalling five lots of AIA-PACK HCG Calibrator Sets because decreased stability may cause measured HCG concentrations to be up to 20% lower than actual.
Product
Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for BHCG Part number 020361 The AIA-Pack BHCG Calibrator Set is intended for IN VITRO DIAGNOSTIC USE ONLY for the calibration of the ST AIA-PACK BHCG assay
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2958-2020·2020-09-23
Boston Scientific Recalls Mislabeled WallFlex Biliary Stent Systems
Boston Scientific is recalling 40 units of WallFlex Biliary RX stents that were mislabeled as fully covered devices. The error involves the 10mm x 60mm size.
Product
WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent) UPN: M00570370 - Product Usage: is indicated for use in the palliative treatment of biliary strictures produced by malignant neoplasms and relief of malignant biliary obstruction prior to surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1522-2020·2020-09-23
Herr's Potato Chips Recalled for Undeclared Allergens and Ingredients
Herr Foods Inc is recalling GameDay Tailgate Tacos Flavored Potato Chips due to undeclared black bean powder, jalapeno pepper powder, paprika, and other ingredients.
Product
Herr s GameDay Tailgate Tacos Flavored Potato Chips 6.5 oz. packaged in a flexible metalized bag. UPC Code: 7260006434
Category
Food
Distribution
6 states
ModerateFDA (Drugs)·D-1605-2020·2020-09-23
RLC Labs Recalls Nature-Throid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions associated with subpotent products.
Product
Nature-Throid, Thyroid USP [liothyronine (T3) 27 mcg and levothyroxine (T4) 114 mcg], 3 Grain (195 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3312-4; b) 60-count bottles, NDC 64727-3312-5; c) 90-count bottles, NDC 64727-3312-6; d) 100-count bottles, NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2959-2020·2020-09-23
Terumo Ultrasonic Air Sensor Recall Due to Intermittent Connection
Terumo is recalling 100 Ultrasonic Air Sensors because a manufacturing defect may cause false air bubble alarms during extracorporeal procedures.
Product
Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32, Catalog Number 5773 - Product Usage: intended for use with Terumo and Sarns brand air detection and heart-lung systems to detect gross air bubbles in the line during extracorporeal procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1602-2020·2020-09-23
RLC Labs Recalls Nature-Throid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions found to be subpotent.
Product
Nature-Throid, Thyroid USP [liothyronine (T3) 18 mcg and levothyroxine (T4) 76 mcg], 2 Grain (130 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3308-4; b) 60-count bottles, NDC 64727-3308-5; c) 90-count bottles, NDC 64727-3308-6; d) 100-count bottles, NDC 64727-3308-1…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2968-2020·2020-09-23
Tosoh Bioscience Recalls AIA-PACK BHCG Calibration Sets Due to Stability Issues
Tosoh Bioscience is recalling 39 boxes of AIA-PACK BHCG Calibration Sets due to decreased stability that may cause inaccurate HCG concentration measurements.
Product
Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro Diagnostic for BHCG-pregnancy Part number: 020661 The AIA-Pack BHCG Calibrator Set is intended for IN VITRO DIAGNOSTIC USE ONLY for the calibration of the ST AIA-PACK BHCG assay
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1604-2020·2020-09-23
RLC Labs Recalls Nature-Throid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions associated with subpotency. The recall covers all lots with expiry dates between October 2020 and July 2023.
Product
Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 mcg], 2.5 Grain (162.5 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3310-4; b) 60-count bottles, NDC 64727-3310-5; c) 90-count bottles, NDC 64727-3310-6; d) 100-count bottles, NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1612-2020·2020-09-23
RLC Labs Recalls WP Thyroid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions associated with subpotent products.
Product
WP Thyroid, Westhroid Pure, 1.75 Grain (113.75 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-6150-2 ; b) 30 Tablets, NDC 64727-6150-4; c) 60 Tablets, NDC 64727-6150-5; d) 90 Tablets, NDC 64727-6150-6; e) 100 Tablets, NDC 64727-6150-1; Rx only, Manufactured by: RLC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1596-2020·2020-09-23
RLC Labs Recalls Nature-Throid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions found to be subpotent.
Product
Nature-Throid, Thyroid USP [liothyronine (T3) 9 mcg and levothyroxine (T4) 38 mcg], 1 Grain (65 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3300-4; b) 60-count bottles, NDC 64727-3300-5; c) 90-count bottles, NDC 64727-3300-6; d) 100-count bottles, NDC 64727-3300-1…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1609-2020·2020-09-23
RLC Labs Recalls WP Thyroid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions found to be subpotent. The recall covers lots expiring between October 2020 and July 2023.
Product
WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-5750-2 ; b) 30 Tablets, NDC 64727-5750-4; c) 60 Tablets, NDC 64727-5750-5; d) 90 Tablets, NDC 64727-5750-6; e) 100 Tablets, NDC 64727-5750-1; Rx only, Manufactured by: RLC Labs…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1610-2020·2020-09-23
RLC Labs Recalls WP Thyroid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions found to be subpotent. The recall covers lots expiring between October 2020 and July 2023.
Product
WP Thyroid, Westhroid Pure, 1.25 Grain (81.25 mg) Thyroid USP packaged in a) 1,000 Tablets, NDC 64727-6050-2 ; b) 30 Tablets, NDC 64727-6050-4; c) 60 Tablets, NDC 64727-6050-5; d) 90 Tablets, NDC 64727-6050-6; e) 100 Tablets, NDC 64727-6050-1; Rx only, Manufactured by: RLC Labs…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2962-2020·2020-09-23
Randox Lactate Dehydrogenase Reagent Recalled for Carryover Avoidance Steps
Randox Laboratories is recalling Lactate Dehydrogenase reagents to update technical bulletins with additional pipette wash steps to prevent reagent carryover and erroneous test results.
Product
Lactate Dehydrogenase L-P, (LDH) (NAO), Catalog Number LD3842 - Product Usage: device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum and plasma. This product is suitable for use on the RX series instruments which includes the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1613-2020·2020-09-23
RLC Labs Recalls WP Thyroid Tablets Due to CGMP Deviations
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions found to be subpotent. The recall covers lots expiring between October 2020 and July 2023.
Product
WP Thyroid, Westhroid Pure, 2 Grain (130 mg) Thyroid USP packaged in a) 1,000 Tablets, NDC 64727-5950-2 ; b) 30 Tablets, NDC 64727-5950-4; c) 60 Tablets, NDC 64727-5950-5; d) 90 Tablets, NDC 64727-5950-6; e) 100 Tablets, NDC 64727-5950-1; Rx Only, Manufactured by: RLC Labs…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2977-2020·2020-09-23
Oxford Immunotec T-SPOT.TB50 Tuberculosis Test Kits Recalled for Labeling Error
Oxford Immunotec is recalling T-SPOT.TB50 tuberculosis test kits due to incorrect expiration dates on the test kit and substrate labels.
Product
Model No:T-SPOT.TB50, Catalogue No.: TB.50; UDI: 1505171600004 - Product Usage: intended for use as an aid in the diagnosis of Mycobacterium tuberculosis infection by detecting effector T cells that respond to stimulation by M. tuberculosis antigens ESAT-6 and CFP10, and…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2957-2020·2020-09-23
Maquet Rotaflow System Console Instructions for Use Recall
Maquet Cardiovascular is recalling Instructions for Use for the Rotaflow System Console because the documents reference an incorrect serial number.
Product
Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions for Use - Centrifugal Pump System is a device that uses a method other than revolving rollers to pump the blood through an extracorporeal circuit Material Number: 701043292
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1585-2020·2020-09-23
Exela Pharma Recalls Potassium Acetate Injection Vials Due to Short Fill
Exela Pharma Sciences LLC is voluntarily recalling 23,775 vials of Potassium Acetate Injection, USP due to short fill issues.
Product
Potassium Acetate Injection, USP 40 mEq/20 mL (2 mEq/mL) Single Dose Vials, Rx only, Manufactured By: Exela Pharma Sciences, LLC. Lenoir, NC NDC 51754-2001-4
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2976-2020·2020-09-23
Oxford Immunotec Recalls T-SPOT.TB8 Kits Due to Incorrect Expiration Dates
Oxford Immunotec is recalling 583 T-SPOT.TB8 test kits because they have incorrect expiration dates on the labeling.
Product
Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the diagnosis of Mycobacterium tuberculosis infection by detecting effector T cells that respond to stimulation by M. tuberculosis antigens ESAT-6 and CFP10, and…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V570000·2020-09-22
Nissan Recalls 2020 Altima, Maxima, and Leaf for Rear Window Defect
Nissan is recalling 2020 Altima, Maxima, and Leaf vehicles because the rear window glass may not remain properly secured, increasing crash risk.
Product
NISSAN — NISSAN LEAF, ALTIMA, MAXIMA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V571000·2020-09-22
Pierce Fire Apparatus Recalled for Joystick Controller Defect
Pierce Manufacturing is recalling 2018-2020 Arrow XT, Dash, Enforcer, Impel, Quantum, and Velocity vehicles because the joystick controller may cause the aerial device to move without operator input.
Product
PIERCE — PIERCE QUANTUM, ARROW XT, ENFORCER, IMPEL
Category
Vehicle
Distribution
Distributed nationwide