State

Minnesota product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52276–52300 of 81675

HighFDA (Drugs)·D-1486-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Extended-Release Capsules
Amerisource Health Services is recalling 834 cartons of amphetamine extended-release capsules because blister cavities may contain more than one tablet or capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 10 mg 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2733-2016·2016-09-14
Integra Cranial Access Kits Recalled Due to Potential Sterility Compromise
Integra LifeSciences is recalling Cranial Access Kits because product seals may open during distribution, rendering the devices unsterile.
Product
Integra Cranial Access Kits, Catalogue Nos. INSHITH; INSHITHRZN; INSHITHND
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2746-2016·2016-09-14
Maquet Operating Room Table Connecting Bracket Recall for Welded Joint Failure
Maquet is recalling Connecting Bracket (Fixture) Devices because post-market surveillance reports indicate the welded joint between the square mount and the first fixable swivel joint is broken.
Product
The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element to support ancillary head rests on a Maquet operating room table immediately before, during and after surgical interventions as well as for examination and treatment. The fixture is used to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2065-2016·2016-09-14
Nature Made Adult Gummies Multi Recalled for Possible Salmonella Contamination
Pharmavite is recalling specific lots of Nature Made adult gummies Multi due to possible Salmonella contamination.
Product
Nature Made(R) adult gummies Multi, 90 count, UPC 0-31604-02841-1
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2067-2016·2016-09-14
Nature Made Multi + Omega-3 Recalled for Possible Salmonella Contamination
Pharmavite is recalling specific lots of Nature Made Multi + Omega-3 supplements due to possible Salmonella contamination. Consumers should stop using the affected products.
Product
Nature Made(R) Multi + Omega-3, 150 count, UPC 0-31604-04173-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2079-2016·2016-09-14
Lysander's Premium Teriyaki Marinade Recalled for Undeclared Allergens
Geneva Foods is recalling Lysander's Premium Teriyaki Marinade because it contains undeclared soy, wheat, and sulfites.
Product
Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 units per case. Manufactured by Geneva Foods, LLC.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2725-2016·2016-09-14
Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm
Hospira is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.
Product
Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1484-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Tablets
Amerisource Health Services is recalling 867 cartons of 20 mg amphetamine tablets due to unit dose blister cavities containing more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2081-2016·2016-09-14
Lysander's Bourbon Flavor Rub Recalled for Undeclared Allergens
Geneva Foods is recalling Lysander's All Natural Bourbon Flavor Rub because it contains undeclared soy, wheat, and sulfites.
Product
Lysander's All Natural Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g), foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2066-2016·2016-09-14
Nature Made Adult Gummies Multi Recalled for Possible Salmonella Contamination
Pharmavite is recalling specific lots of Nature Made adult gummies Multi due to possible Salmonella contamination. Consumers should check lot numbers and expiration dates.
Product
Nature Made(R) adult gummies Multi, 150 count, UPC 0-31604-04172-4
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2071-2016·2016-09-14
Nature Made Super B-Complex Recalled for Possible Bacterial Contamination
Pharmavite is recalling Nature Made Super B-Complex vitamins due to possible Staphylococcus aureus and Salmonella contamination in specific lots.
Product
Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 460 count, UPC 0-31604-02728-5
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2072-2016·2016-09-14
Nature Made Super B-Complex Recalled for Possible Bacterial Contamination
Pharmavite is recalling Nature Made Super B-Complex supplements due to possible Staphylococcus aureus and Salmonella contamination in specific lots.
Product
Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 360 count, UPC 0-31604-02729-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2765-2016·2016-09-14
Hologic Recalls SureSight Obturator Introducer Systems Due to Tip Breakage
Hologic is recalling 1,440 SureSight Obturator Introducer Localization Systems because the tip may break at the glue joint.
Product
SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI. ILS-0914-20-OB (9G Introducer Localization Set (OB Model) for ATEC0914-20MR Handpiece)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2737-2016·2016-09-14
Philips BrightView XCT Upgrade Recalled for Potential Patient Contact
Philips is recalling three BrightView XCT Upgrade units due to a software defect that may cause the detector to contact patients during specific scans.
Product
BrightView XCT Upgrade Model 882454
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2729-2016·2016-09-14
Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm
Hospira Inc. is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.
Product
Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2734-2016·2016-09-14
Omega Medical Imaging Recalls Elevating Monitor Suspension Systems
Omega Medical Imaging is recalling 26 Elevating Monitor Suspension Systems because the suspension may separate from the lifting column bracket.
Product
2 over 2 Elevating Monitor Suspension - Omega Medical Imaging, LLC Elevating Monitor Suspension Systems.
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-2738-2016·2016-09-14
Terumo Recalls Pinnacle Introducer Sheaths Due to Valve Leakage
Terumo Medical Corporation is recalling Pinnacle Introducer Sheaths due to a manufacturing issue causing valve leakage, which poses a risk of incremental blood loss.
Product
PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2762-2016·2016-09-14
Riverpoint Medical Recalls Webglo Polypropylene Surgical Sutures Due to Seal Issues
Riverpoint Medical is recalling specific lots of Webglo polypropylene surgical sutures because the seals may open during distribution or packaging.
Product
Polypropylene Surgical Sutures, brand Webglo, for vet use. Product is sterile. Part number: GP8665 Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2763-2016·2016-09-14
Blackrock NeuroPort Biopotential Signal Processing System Recall for Labeling Error
Blackrock Microsystems is recalling 81 Neural Signal Amplifiers because the device and patient cable are incorrectly labeled as Type CF Applied Parts.
Product
Neural Signal Amplifier. Part Numbers: 4208, 5703, 5749, 5748, 5747. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes. Biopotential signals include…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2074-2016·2016-09-14
Nature Made Hair Skin Nails Gummies Recalled for Microbial Count
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Product
Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC 0-31604-04132-8-1
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2764-2016·2016-09-14
Blackrock NeuroPort Patient Cables Recalled for Incorrect Labeling
Blackrock Microsystems is voluntarily recalling 120 Patient Cables because they are incorrectly labeled as Type CF Applied Parts.
Product
Patient Cable. Part Numbers: 4460, 6735. Sterile within Chipboard Boxes within corrugated cartons. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1491-2016·2016-09-14
Zydus Recalls Bromocriptine Mesylate Capsules Due to Stability Test Failures
Zydus Pharmaceuticals is recalling 14,808 bottles of Bromocriptine Mesylate 5 mg capsules because stability samples failed impurity tests.
Product
BROMOCRIPTINE MESYLATE — BROMOCRIPTINE MESYLATE (BROMOCRIPTINE MESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2742-2016·2016-09-14
Siemens ADVIA Centaur PSA Assay Recall for Clinical Interpretation Clarification
Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits to emphasize that PSA values must be interpreted according to current clinical guidelines for biochemical recurrence.
Product
ADVIA Centaur¿ PSA Assay; Cat No. 06574155/SMN 10310292 (100 test)/02676506/SMN 10310293 (500 test)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2073-2016·2016-09-14
Nature Made Hair Skin Nails Gummies Recalled for Microbial Count
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Product
Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC 0-31604-04016-1
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2747-2016·2016-09-14
Mentor Breast Tissue Expanders Recalled Due to Product Mix-Up
Mentor Texas, LP. is recalling 65 units of MENTOR CPX4 breast tissue expanders because a 350cc unit was found in a carton intended for 450cc units.
Product
MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
Category
Medical Device
Distribution
Distributed nationwide