Minnesota recalls
3,519 federal recalls affecting Minnesota in the last 12 months - 156 Minnesota-specific plus 3,363 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-26CPSCSunnyyesNationwideStop using Sunnyyes LED mini lights immediately
Sunnyyes LED mini lights contain lithium coin batteries that children can easily access and swallow. The battery compartment screws can come loose, and the packaging lacks required safety warnings. Swallowing these batteries can cause serious internal burns and death.
- 2026-03-26CPSCDuraTracNationwideStop using DuraTrac gas connectors
DuraTrac stainless steel gas connectors sold between May and November 2025 contain a manufacturing defect that can cause gas leaks. These leaks pose a fire hazard. About 196,800 units are affected.
- 2026-03-26CPSCAirClubNationwideStop using AirClub convertible bassinets immediately
AirClub convertible bassinets (model QX-831) have a defective attachment mechanism that creates a dangerous gap between the bassinet and adult bed mattress. Infants can fall through this opening, causing serious injury or death. About 110,400 units were sold online between October 2023 and December 2025.
- 2026-03-26CPSCVive HealthNationwideStop using Vive Health bed rails immediately
Vive Health bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. Two deaths have been reported. The recall affects three models: Compact Bed Rail (LVA2009SLV), Bed Rail Collection V (LVA2097SLV), and Bed Rail model LVA1024 purchased on or before August 21, 2023.
- 2026-03-26CPSC4our KiddiesNationwideStop using 4our Kiddies furniture straps immediately
4our Kiddies plastic furniture straps (tip restraint kits) can break or degrade over time, allowing furniture to tip over and potentially trap or injure children or elderly people. The plastic brackets and cables fail to meet safety standards, and CPSC has received reports of at least 150 incidents where these straps broke, including three furniture tip-overs.
- 2026-03-26CPSCNexgrillNationwideStop using Nexgrill grill brushes immediately
Nexgrill grill brushes sold at Home Depot can shed small metal wire bristles that may stick to food or the grill surface. If swallowed, these bristles can cause serious internal injuries requiring surgery. The company has identified at least 68 cases where bristles detached, including five people who needed medical care.
- 2026-03-25FDA-DeviceDatascopeClass IIINationwideCheck your Datascope battery charger left bay
Datascope's Battery Charging Station (Model 0998-00-0802) for Cardiosave IABP batteries has a protruding screw in the left bay that can prevent certain batteries from inserting fully and charging properly. The right bay works normally. This affects 28 units distributed in select U.S. states and international locations.
- 2026-03-25FDA-DeviceHologicClass IINationwideStop using Hologic Aptima HPV Assay kits
Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.
- 2026-03-25FDA-DeviceDiagnostica StagoClass IINationwideStop using STA Liatest D-Di test kits
Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.
- 2026-03-25FDA-DeviceConvaTecClass IINationwideStop using ConvaTec EsteemBody Drainable Pouch
ConvaTec has recalled certain EsteemBody Drainable Pouches (REF: 423657, 10-35mm) because they may leak due to a manufacturing issue. The affected pouches have lot number 5J03908. No injuries have been reported.
- 2026-03-25FDA-DeviceConvaTecClass IINationwideStop using ConvaTec EsteemBody Drainable Pouch
ConvaTec has recalled certain EsteemBody Drainable Pouches (model REF:423653, 10-35mm) because they may leak due to a manufacturing issue. The affected product has lot number 5K01728. No injuries have been reported.
- 2026-03-25FDA-DeviceConvaTecClass IINationwideStop using ConvaTec EsteemBody Drainable Pouch
ConvaTec's EsteemBody Drainable Pouch (model REF:423643, 10–45mm) may leak because of a manufacturing issue. The affected pouches have lot numbers 5K00011 or 5K00714 and have been distributed worldwide. No injuries have been reported.
- 2026-03-25FDA-DeviceElektaClass IINationwideCheck your Leksell Gamma Knife serial number
Elekta has recalled certain Leksell Gamma Knife Perfexion and Icon radiosurgery systems because an adapter component may not be properly aligned or locked in place. This could affect the accuracy of radiation delivery during treatment. No injuries have been reported.
- 2026-03-25FDA-DeviceStrykerClass IINationwideCheck your Stryker Cub crib serial number
Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.
- 2026-03-25FDA-DeviceLeMaitre VascularClass IINationwideCheck LeMaitre Vascular Artegraft Graft packaging
LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.
- 2026-03-25FDA-DeviceBaxterClass IINationwideStop using Welch Allyn Vision Screener VS100
The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.
- 2026-03-25FDA-DeviceHowmedica OsteonicsClass IINationwideStop using Howmedica MICS3 Saw Attachment
The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
GE Medical Systems' Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 has a cybersecurity weakness that may expose user login credentials on affected workstations. An unauthorized person could potentially use these exposed credentials to access the system, disrupt service, or alter medical images and data.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
Certain versions of GE Centricity Universal Viewer software (versions 6.0 through 6.0 Sp10.4.1) contain a cybersecurity vulnerability that may expose user login credentials on affected workstations. An unauthorized person could potentially access the system and interfere with medical imaging data or system availability.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
Certain versions of GE Centricity Universal Viewer software (versions 7.0 through 7.0 Sp2.0.1) contain a cybersecurity vulnerability that may expose user login credentials on workstations. An unauthorized person could potentially access the system and disrupt service or alter medical image data.
- 2026-03-25FDA-DeviceAbbottClass IINationwideStop using Abbott ID NOW flu test kit
Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.
- 2026-03-25USDAPublic Health AlertNationwideDo not eat Blackwing Organic Meats beef or pork
Blackwing Organic Meats sold beef and pork products that were produced without required federal inspection and some bear false USDA inspection marks. These products may contain harmful bacteria, allergens, or other contaminants. The affected products were produced between April 2024 and March 2026 and shipped nationwide.
- 2026-03-25FDA-FoodKradjianClass INationwideStop using MID EAST Jordanian Zaatar spice mix
MID EAST Jordanian Zaatar spice mix in 5 lb bags contains sesame and wheat that are not listed on the label. This product was distributed to bakeries for use in breads and pastries. People with sesame or wheat allergies could have a serious reaction if they consume products made with this spice mix.
- 2026-03-25FDA-DrugApotexClass IINationwideStop using Apotex brimonidine/timolol eye drops
Apotex Corp. is recalling specific lots of brimonidine tartrate/timolol maleate eye drops because the manufacturer cannot confirm the product was sterilized properly. The affected lots are VJ8599 (expires 09/30/2026) and VL1668 (expires 01/31/2027). No infections or injuries have been reported so far.
- 2026-03-25FDA-DrugSomerset TherapeuticsClass IINationwideStop using Somerset Therapeutics dexamethasone injection
Somerset Therapeutics is recalling one lot of dexamethasone sodium phosphate injection because testing found impurity levels above acceptable limits as the product approached its expiration date. The affected lot (A240421, expiring 07/31/2026) was distributed nationwide. No injuries have been reported.
- 2026-03-25FDA-DrugStridesClass IINationwideStop using Strides Pharma Children's Ibuprofen
Strides Pharma Children's Ibuprofen Oral Suspension (100 mg per 5 mL) has been recalled because some bottles contain gel-like masses and black particles. The affected bottles are 4 FL OZ (120 mL) size with lot numbers 7261973A or 7261974A, expiring 01/31/2027. No injuries have been reported.
- 2026-03-25FDA-FoodShaman BotanicalsClass INationwideStop using Shaman Botanicals White Vein tablets
Shaman Botanicals is recalling White Vein Advanced Alkaloids chewable tablets because testing found the active ingredient (7-hydroxymitragynine) is present in higher amounts than stated on the label. The label says 7.5 mg per serving, but the actual content is greater. No injuries have been reported.
- 2026-03-24FDA-PRAmneal PharmaceuticalsNationwideStop using Amneal Magnesium Sulfate IV bags
One lot of Amneal Magnesium Sulfate in Water for Injection IV bags was found to contain the wrong medication—Tranexamic Acid—inside the packaging. This mix-up affects hospitals that received the product between late December 2025 and late February 2026. No patients have been harmed so far.
- 2026-03-19CPSCYxtdz StoreNationwideStop using Aisstxoer bicycle helmets immediately
Aisstxoer brand adult bicycle helmets sold on Amazon do not meet safety standards for impact protection and fit stability. If you crash while wearing one, the helmet may fail to protect your head, risking serious injury or death.
- 2026-03-19CPSCAmazonNationwideStop using Amazon Basics pocket knife
The blade on Amazon Basics Camping Folding Pocket Knives can fail to stay closed, creating a risk of cuts. Amazon received one report of the blade opening unexpectedly, though no injuries have been reported so far.
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