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.

57001–57025 of 81684

ModerateFDA (Devices)·Z-0278-2016·2015-11-25
Ethicon Harmonic ACE+ 7 Laparoscopic Shears Recalled for Packaging Defect
Ethicon Endo-Surgery is recalling Harmonic ACE+ 7 Laparoscopic Shears because holes in the Tyvek packaging can compromise the sterile barrier.
Product
HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm, 36cm, 45cm length), Ethicon Endo-Surgery. Indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0234-2016·2015-11-25
Par Pharmaceutical Recalls Meclizine Hydrochloride Tablets Due to Impurity Failures
Par Pharmaceutical is recalling Meclizine Hydrochloride Tablets because they failed impurity specifications. The recall covers 100 and 1000-count bottles distributed nationwide.
Product
Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-035-01) and b) 1000 Ct Bottles (NDC: 49884-035-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0300-2016·2015-11-25
Ameditech Recalls 11 Panel Drug Abuse Tests Due to Reduced Reactivity
Ameditech is recalling 11 Panel Drug Abuse Tests because they have shown reduced reactivity. The affected products are distributed in the US and Australia.
Product
11 Panel Cup (OPI2000) w/Adult, Item No. 71125AA2K ; and 11 Panel Cup (OPI300) w/Adult, Item No. 71125AA These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0303-2016·2015-11-25
Ameditech Recalls ArcPoint Labs 10 Panel Dip Screen Due to Reduced Reactivity
Ameditech is recalling ArcPoint Labs 10 Panel Dip Screen (OXY) drug tests because they have shown reduced reactivity.
Product
ArcPoint Labs 10 Panel Dip Screen (OXY), Item No. APD-10MO These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0315-2016·2015-11-25
Ameditech Recalls ProScreen Drug Panel Tests Due to Reduced Reactivity
Ameditech is recalling ProScreen drug panel tests because they have shown reduced reactivity. The recall covers 31,530 units distributed in the US and Australia.
Product
ProScreen 10 Drug Panel Cassette Test, Item No. CPSP-10PPX; ProScreen 10 Panel Cup, Item No. PSCup-10MMO-300, PSCup-10M, PSCupA-10MO, PSCUp-10AB; ProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM; ProScreen 10 Panel Dip Card, Item No. PSD-10MMO-300, PSD-10MOX…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0304-2016·2015-11-25
Ameditech Recalls CLIA RDTC 12-Panel Drug Abuse Tests for Reduced Reactivity
Ameditech is recalling 7,482 units of CLIA RDTC 12-Panel Cup drug abuse tests because they have shown reduced reactivity. The products were distributed in the US and Australia.
Product
CLIA RDTC 12-Panel Cup and CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12 These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0317-2016·2015-11-25
Ameditech Recalls Thermo Fisher 6 Drug Cassettes Due to Reduced Reactivity
Ameditech is recalling Thermo Fisher 6 Drug Cassettes because they have shown reduced reactivity. The recall affects 220 units distributed in the US and Australia.
Product
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU, MTPA-8MBAU These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0309-2016·2015-11-25
Ameditech Recalls DrugSmart Dip Drug Abuse Tests Due to Reduced Reactivity
Ameditech is recalling 160 units of DrugSmart Dip drug abuse tests because they have shown reduced reactivity. The affected products were distributed in the US and Australia.
Product
DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D; DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0187-2016·2015-11-25
Herr's Potato Chips Recalled for Incorrect Gluten-Free Labeling
Herr's Foods is recalling Sour Cream & Onion Potato Chips because packaging incorrectly states the product is gluten-free, despite containing wheat.
Product
Herr's Sour Cream & Onion Flavored Potato Chips
Category
Food
Distribution
21 states
ModerateFDA (Devices)·Z-0308-2016·2015-11-25
Ameditech Recalls DrugSmart Drug Abuse Test Cups Due to Reduced Reactivity
Ameditech is recalling specific DrugSmart drug abuse test cups because they have shown reduced reactivity. The affected units were distributed in the US and Australia.
Product
DrugSmart 11 Test Cup, Item No. 61127D; DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D; DrugSmart 9 Test Cup (BUP), Item No. 60960D; DrugSmart Cup 10, Item No. 61093D-3C These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0314-2016·2015-11-25
Ameditech Recalls Premier Clia Waived 12 Panel Tilt Cup Drug Tests
Ameditech is recalling Premier Clia Waived 12 Panel Tilt Cup drug tests because they have shown reduced reactivity.
Product
Premier Clia Waived 12 panel Tilt Cup, Item No. C12APC These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0316-2016·2015-11-25
Ameditech Recalls 6 Panel Drug Detection Cups Due to Reduced Reactivity
Ameditech is recalling 2,240 units of 6 Panel Cup Body and Lid drug tests because they have shown reduced reactivity.
Product
The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0307-2016·2015-11-25
Ameditech Recalls DrugSmart 10 Test Cups Due to Reduced Reactivity
Ameditech is recalling DrugSmart 10 Test Cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Product
DrugSmart 10 Test Cup (PCP & MDMA), Item No. 61055D; DrugSmart 10 Test Cup (PCP & OXY), Item No. 61020D These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0299-2016·2015-11-25
Ameditech Recalls 10-Panel Pipette Drug Screen Due to Reduced Reactivity
Ameditech is recalling 10-Panel Pipette Drug Screen tests because they have shown reduced reactivity. The recall affects 200 units distributed in the US and Australia.
Product
10-Panel Pipette Drug Screen, Item No. PSP-10M These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0305-2016·2015-11-25
Ameditech Recalls DrugCheck Pipette 10 Drug Tests Due to Reduced Reactivity
Ameditech is recalling 70 units of DrugCheck Pipette 10 Drug Tests because they have shown reduced reactivity. The affected tests were distributed in the US and Australia.
Product
DrugCheck Pipette 10 Drug Test, Item No. 41025 DC These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0235-2016·2015-11-25
Mylan Recalls Meclizine Hydrochloride Tablets Due to Impurity Failures
Mylan Institutional is recalling 4,609 packages of Meclizine Hydrochloride 25 mg tablets because they failed impurity specifications.
Product
Meclizine Hydrochloride Tablets, USP, 25 mg Tablets, Packaged in 10 x 10 Tablet Blister Pack Packages, Rx Only. Manufactured by: Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977. Mylan. NDC: 51079-090-20.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0302-2016·2015-11-25
Ameditech Recalls 12-Panel Dip Drug Screens Due to Reduced Reactivity
Ameditech is recalling 12-Panel Dip Drug Screens with adulterant because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Product
12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0295-2016·2015-11-25
Akorn Recalls Hydrocortisone Otic Solution Due to Missing Safety Seal
Akorn, Inc. is recalling 13,896 bottles of Hydrocortisone and Acetic Acid Otic Solution because the bottles are missing the safety seal around the neck.
Product
Hydrocortisone and Acetic Acid Otic Solution, USP, containing hydrocortisone (1%) and acetic acid (2%), 10 mL bottles, Rx Only, Hi-Tech Pharmacal, Amityville, NY 11701, Made in USA, NDC # 50383-901-10
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0231-2016·2015-11-25
Akorn Recalls RIFAMPIN FOR INJECTION Due to Impurity Specifications
Akorn, Inc. is recalling 6,861 vials of RIFAMPIN FOR INJECTION USP, 600 mg because a known impurity failed to meet specifications.
Product
RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0233-2016·2015-11-25
Par Pharmaceutical Recalls Meclizine Hydrochloride Tablets Due to Impurities
Par Pharmaceutical is recalling specific lots of Meclizine Hydrochloride 12.5 mg tablets because they failed impurity specifications.
Product
Meclizine Hydrochloride Tablets, USP, 12.5 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-034-01) and b) 1000 Ct Bottles (NDC: 49884-034-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0291-2016·2015-11-25
Baxter HomeChoice APD Systems Recalled for Loud Operating Sounds
Baxter is recalling HomeChoice and HomeChoice Pro APD systems due to loud operating sounds. The devices function correctly, but the noise is unacceptable to users.
Product
Baxter HomeChoice and HomeChoice Pro APD systems, designed to provide Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V796000·2015-11-24
Mercedes-Benz Recalls 2015 S550E Hybrid Vehicles Due to Charger Defect
Mercedes-Benz is recalling 2015 S550E Hybrid vehicles because a defective onboard charger may cause the car to unexpectedly shift to park, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ S550E
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V792000·2015-11-24
Mercedes-Benz Recalls 2014 E350 Sedans for Fuel Line Fire Risk
Mercedes-Benz is recalling 809 model year 2014 E350 sedans because a fuel feed line defect may cause a leak or disconnection, increasing the risk of fire or a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ E350
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16045·2015-11-24
SalesOne Recalls Light Up Ear Plug Jewelry Due to Burn Hazard
SalesOne is recalling light-up ear plug jewelry sold at Spencer Gifts because battery acid can leak and cause burns. Consumers should stop wearing the product and contact SalesOne for a refund or replacement.
Product
Light up ear plug jewelry
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·15V791000·2015-11-24
Wabash National Van Trailers Recalled for Brake Caliper Bolt Defect
Wabash is recalling 2013-2015 Van Trailers because brake caliper bolts may not be tightened, risking caliper detachment and reduced braking.
Product
WABASH NATIONAL — WABASH NATIONAL VAN
Category
Vehicle
Distribution
Distributed nationwide