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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 48,759 notices were distributed nationwide, so they reach Iowa too — those are in the archive.

Medical devices

Reported Jun 11, 2025

Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Silex Medical, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 4, 2025

Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 4, 2025

Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2025

Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8"…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

C.R. Bard Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2025

META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Food

Reported May 28, 2025

Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Vietti Acquisitions, LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 21, 2025

LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 21, 2025

Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Meddev Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 14, 2025

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported May 14, 2025

Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz., in clear plastic clamshell container, UPC 00773164

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Taylor Farms Illinois Inc.

FDA (openFDA food enforcement)

Food

Reported May 7, 2025

Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dianne's Fine Desserts

FDA (openFDA food enforcement)

Medical devices

Reported May 7, 2025

Enhanced Verify Evaluation Handset (CFN HH90130FA)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ihb Operations B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 30, 2025

Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

S Martinelli & Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 23, 2025

Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Avanos Medical, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Maquet Cardiovascular, LLC

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.