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 May 26, 2021
REF 7617400, Groshong NXT ClearVue Catheter, intermediate kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741045094 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported May 26, 2021
ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hi Tech Pharmaceuticals
13 more products in this recall
FDA (openFDA food enforcement)
Reported May 26, 2021
Newly Weds A70088 bread crumbs X1, 35lbs bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Newly Weds Foods Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported May 26, 2021
PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Public Goods
FDA (openFDA food enforcement)
Reported May 26, 2021
Veggie Pizza sold under the following brands: Crazy Fresh, quick & easy, and blank label. Item # 81068, Net Wt. 6.2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Russ Davis Wholesale Inc.
FDA (openFDA food enforcement)
Reported May 19, 2021
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 19, 2021
Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported May 19, 2021
ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St. Jude Medical, Cardian Rhythm Management Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 19, 2021
Alaris Pump Module, Model 8100, serviced/repaired by Step-Har Medical with an impacted bezel repair part
High riskUsing this product could cause serious injury, illness or death — stop using it now.Step-Har Medical LLC
FDA (openFDA device enforcement)
Reported May 12, 2021
Hostesss SnoBalls packaged as Hostess Chocolate CupCakes, Net Wt 3.17 OZ, UPC 8 88109 01001 0, Hostess Brands, LLC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands LLC
FDA (openFDA food enforcement)
Reported May 12, 2021
Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natrol, LLC
FDA (openFDA food enforcement)
Reported May 12, 2021
Grace Medical REF S-2500 *** SHEEHY BONE DUST COLLECTOR *** Stainless steel filter - Product Usage: intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oto Med Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 5, 2021
Change Healthcare Enterprise Viewer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Canada Company
FDA (openFDA device enforcement)
Reported May 5, 2021
Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cytocell Ltd.
FDA (openFDA device enforcement)
Reported May 5, 2021
InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product Usage: Intended as a three-part construct…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 5, 2021
Tuscan Garden Ranch Dressing, packaged in 16 oz bottles, Dist. & Sold Exclusively by ALDI, Batavia, IL packaged in 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richelieu Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 28, 2021
The AMS 700 Inflatable Penile Prosthesis is a closed fluid-filled system containing saline. The system is made out of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Apr 28, 2021
BCS XP System: Multipurpose system for in vitro coagulation studies. Product code: 10459330, 10461894, 10470625 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Midline Catheter Dressing Change Kit with Statlock - Product Usage: Intended to provide ongoing vascular catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trinity Sterile, Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
KeVita Cucumber Rosemary (primary package), 15.2 oz., glass bottles, 6 packages per case, refrigerated storage
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tropicana Products, Inc.
FDA (openFDA food enforcement)
Reported Apr 21, 2021
MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
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.