Recalls distributed in Minnesota
These notices name Minnesota in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
3,845 stored notices name Minnesota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.
Reported Mar 15, 2023
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linet Spol. S.r.o.
FDA (openFDA device enforcement)
Reported Mar 15, 2023
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Preat Corp.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alpenland International, Inc.
FDA (openFDA food enforcement)
Reported Mar 8, 2023
Ultracell Wick with 80cc Collection Bag, 20/box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec International, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
EMPOWR VVC KNEE TIBIAL INSERT, SIZE 6, 22MM, REF: 346-22-706; EMPOWR VVC KNEE TIBIAL INSERT, SIZE 7, 22MM, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Mar 1, 2023
abm Respiratory Care Standart Breating Circuit with Face Mask - Toddler REF BC21087 abm Respiratory Care Standart…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.S & Mohr America, S.a. de C.v.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
Super Size Golden Harvest Carrot Cate, Item 06233. Net 9.8 kg 345 oz (21 lb 9 oz). UPC 7 70118-06233 6. Keep Frozen.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Original Cakerie Ltd.
FDA (openFDA food enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
AxiEM" Non-Invasive Patient Tracker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Veritas Advanced Infusion Packs, REF: VRT-AI
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2023
Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jan 25, 2023
Rasagiline Mesylate Tablets 1 mg; 30 tablets in HDPE bottle; Rx only; NDC 67877-260-30; Manufactured by Alkem…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Jan 18, 2023
Source Administration Set (SAS) used with the Medrad Intego PET Infusion System, Sterile Catalog number: INT CSS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
BD Pyxis MedBank System - Product Label/labeling pending
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Beijing Hawthorne Candy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
Three Gold Coins, Dried Mushrooms Sliced (01051) Nam Meo Soi S- 50x2.5 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tai Phat Wholesalers LLC
3 more products in this recall
FDA (openFDA food enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.