Recalls distributed in Iowa
These notices name Iowa 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.
2,881 stored notices name Iowa, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Iowa too — those are in the archive.
In the agency's Nov 11, 2026 enforcement report
Nextseq 550Dx Instrument REF: 20005715, FOR IN VITRO DIAGNOSTIC USE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
2 more products in this recall
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
Tandem Mobi Insulin Pump, Models: 1004004, 1010750, 1012676, 1012719, 1013655, 1013656, 1013501, 1013700, 1014081,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
EDEN BROTHERS Broccoli Seeds - Calabrese. Sold in packets, Net Wt. 1oz pouches, UPC SVBRO111 -qb2 & 1 Pound pouches UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eden Brothers
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Miyoko's Creamery European Style Salted Plant Milk Butter, Net Wt. 8 OZ (227G). UPC 857554005773. Distributed By:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prosperity Organic Foods Inc.
FDA (weekly enforcement report)
Reported Oct 28, 2026Updated Nov 2, 2026
PNE Lead Implant Kit REF: 1701
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Axonics, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Philips Lumify Diagnostic Ultrasound System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Oct 24, 2026
Imperio Distribution LLC Recalls Beef Jerky Products Produced Without the Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Imperio Distribution LLC
USDA FSIS
Reported Oct 21, 2026Updated Oct 26, 2026
Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Nov 2, 2026
Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sarnova HC, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G L Mezzetta Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safeguard US Operating LLC
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
In-Line Valve, Product Number: P5-TEE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Percussionaire Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Iowa recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.