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.
2,845 stored notices name Iowa, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Iowa too — those are in the archive.
Reported Mar 26, 2025
Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oridion Medical 1987 Ltd.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. Dist. By Target Corporation, Minneapolis,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Foods, Inc.
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruAbutment Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Paradigm REF: MMT-712 and MMT-715
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Philips IntelliSpace Cardiovascular software, Model 830089.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.V.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Noble Made Garlic Parmesan Wing Sauce, net wt 9.25oz, UPC 850000398542, #0897 BEST BY 06/02/2026 14:02 33724 L1, Code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spicin Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 5, 2025
BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2025
Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nestle-USA, Inc. (Corporate Office)
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 26, 2025
Jack & the Green Sprouts Alfalfa Sprouts. Net Weight 5 oz. (152g). UPC 7 63247-19891 5. Keep Refrigerated. Product of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jack & The Green Sprouts, Inc.
FDA (openFDA food enforcement)
Reported Feb 26, 2025
3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kci USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2025
LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2025
MOSAIQ Oncology Information System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2025
Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Feb 19, 2025
Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co. LLC
FDA (openFDA device enforcement)
Reported Feb 19, 2025
Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Feb 19, 2025
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Max Mobility LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
NuGo Dark Chocolate Pretzel with Sea Salt , Real Dark Chocolate / Vegan. 12g Protein
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bazzini LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2025
Temporary Titanium Abutments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DDS Lab
FDA (openFDA device enforcement)
Reported Feb 12, 2025
PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2025
The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2025
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
FDA (openFDA device 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.