State

Iowa product recalls

73,190 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total: 5,590
Critical: 910
Severe: 1,320
Most recent: 2026-09-30

Of the 5,590 recalls naming Iowa we have scored against our rubric, 910 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,320 (24%) are Severe.

Which agencies issued them

These figures cover only the 5,590 recalls whose distribution notice names Iowa specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13726–13750 of 78780

SevereFDA (Food)·F-0700-2024·2024-01-17
Eban's Bakehouse Turtle Brownie Cookies Recalled for Undeclared Milk and Soy
Eban's Bakehouse LLC is recalling Turtle Brownie cookies that contain undeclared milk and soy allergens. Consumers with allergies should not consume the product.
Product
Eban's Bakehouse Sweet Indulgences - Turtle Brownie (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
Category
Food
Distribution
33 states
SevereFDA (Food)·F-0695-2024·2024-01-17
Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens
Eban's Bakehouse Sweet Indulgences cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies should not consume these products and should discard or return them.
Product
Eban's Bakehouse Sweet Indulgences - Brown Butter Honey Pistachio (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
Category
Food
Distribution
33 states
SevereFDA (Food)·F-0699-2024·2024-01-17
Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens
Eban's Bakehouse Sweet Indulgences cookies are recalled due to undeclared milk and soy allergens not listed on the label. Consumers with allergies to milk or soy should not consume this product.
Product
Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate Chunk (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
Category
Food
Distribution
33 states
SevereFDA (Food)·F-0698-2024·2024-01-17
Eban's Bakehouse Lemon Sugar Cookies Recalled for Undeclared Milk and Soy
Eban's Bakehouse Sweet Indulgences lemon cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Product
Eban's Bakehouse Sweet Indulgences - Lemon Sugar Cookie/Lemon Shortbread (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
Category
Food
Distribution
33 states
SevereFDA (Drugs)·D-0220-2024·2024-01-17
Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk
InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.
Product
VIGABATRIN — VIGABATRIN (VIGABATRIN)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V020000·2024-01-17
Morgan Super 3 motorcycles recalled for brake master cylinder weld defect
Morgan Motor Company is recalling 2023 Super 3 motorcycles because a defective weld may cause brake failure. Owners should contact the manufacturer for a free repair.
Product
MORGAN MOTOR COMPANY — MORGAN MOTOR COMPANY SUPER 3
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0694-2024·2024-01-17
Eban's Bakehouse Sweet Indulgences cookies recalled for undeclared milk and soy
Eban's Bakehouse LLC is recalling Sweet Indulgences cookies for containing undeclared milk and soy allergens, which pose serious health risks to allergic consumers.
Product
Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
Category
Food
Distribution
33 states
SevereFDA (Food)·F-0701-2024·2024-01-17
FDA recalls Chocolate Fudge for undeclared egg allergen
Valley View Candies recalled Chocolate Fudge due to undeclared egg allergen. The recall affects 348 containers distributed to retail stores in Iowa.
Product
Chocolate Fudge, 8oz, packaged in clear, plastic clamshell.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0704-2024·2024-01-17
Peanut Butter Fudge Recalled for Undeclared Egg Allergen
All lots of Peanut Butter Fudge sold in Iowa are recalled due to undeclared egg allergen. The manufacturer initiated the voluntary recall.
Product
Peanut Butter Fudge, 8oz, packaged in clear, plastic clamshell.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0691-2024·2024-01-17
VISERA Cysto-Nephro Videoscope Model CYF-V2: Reusable Brush Cleaning Update
Olympus is updating instructions for the VISERA Cysto-Nephro Videoscope (Model CYF-V2) nationwide, removing reusable brushes from manual cleaning procedures. Single-use brushes remain compatible.
Product
Model No. CYF-V2, VISERA Cysto-Nephro Videoscope
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0643-2024·2024-01-17
Bard Mission Biopsy Instrument Kits Recalled for Improper Needle-Cannula Fit
Bard is recalling Mission Disposable Core Biopsy Instrument Kits due to dimensional issues that may prevent the biopsy needle from fitting properly into the cannula, potentially causing tissue injury and prolonging procedures.
Product
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM; 1610MSK/ Mission Kit 16G x 10CM; 1616MSK/ Mission Kit 16G x 16CM; 1810MSK/ Mission Kit 18G x 10CM; 1816MSK/ Mission Kit 18G x 16CM; 1820MSK/ Mission…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0672-2024·2024-01-17
SPRYSTEP VECTOR KAFO ankle-foot orthosis recalled for structural failure risk
The SPRYSTEP VECTOR KAFO custom ankle-foot orthosis is being recalled by Townsend Design due to air pockets that could cause complete structural failure.
Product
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
Category
Medical Device
Distribution
48 states
HighFDA (Devices)·Z-0714-2024·2024-01-17
Ambu aView 2 Monitor recalled for fire and burn hazard from oversized mounting screws
Ambu is recalling the aView 2 A Monitor due to fire and burn hazards if mounting screws longer than 16mm are used. Improper installation can penetrate the lithium-ion battery, causing fires, severe burns, and smoke inhalation.
Product
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0697-2024·2024-01-17
Olympus ENDOEYE HD II Videoscope Image Discoloration Recall
Two Olympus ENDOEYE HD II Rigid Videoscope catalog numbers (WA50040A, WA50042A) have been recalled due to reports of pink or green image discoloration during use. The issue could require device exchange during surgery and potentially result in visual impacts or bleeding.
Product
Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A, WA50042A -used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V018000·2024-01-17
Heartland Recalls 2024 Corterra Fifth Wheels for Incorrect Tire Labels
Heartland is recalling 2024 Corterra fifth wheels because certification labels may have missing or incorrect tire size information, potentially leading to the installation of wrong tires.
Product
HEARTLAND — HEARTLAND CORTERRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0698-2024·2024-01-17
Medtronic Percutaneous Surgical Pins Recalled Due to Potential Fitting Defects
Medtronic is recalling 4,235 percutaneous surgical pins that may have a manufacturing defect preventing proper fit into or removal from the tap cap. The pins were distributed nationwide and internationally.
Product
Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0677-2024·2024-01-17
Philips BrightView Gamma Camera System Recalled for Extremity Entrapment Hazard
Philips is recalling BrightView Gamma Camera Systems because a gap can form between patient support and detector during quality assurance scans, creating an extremity entrapment hazard that may cause fractures or crush injuries.
Product
BrightView, Gamma Camera System, Product Code 882480.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0676-2024·2024-01-17
BD Recanalization System May Overheat or Break During Use
Bard Peripheral Vascular is recalling BD Recanalization Systems due to a manufacturing defect that may allow continuous operation without required safety warnings, increasing risk of device overheating or breaking during patient treatment.
Product
BD Recanalization System, REF: BDRECANSYSTEM
Category
Medical Device
Distribution
34 states
HighFDA (Devices)·Z-0640-2024·2024-01-17
Philips Incisive CT Scanner Software Issues May Cause Misdiagnosis
Philips is recalling Incisive CT scanners due to nine software defects including image artifacts, incorrect orientation labels, display failures, and positioning errors that could lead to misdiagnosis or need for rescans. No illnesses have been reported.
Product
Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0641-2024·2024-01-17
Medical diagnostic reagent recall: incorrect cell staining fluorescence
BD Biosciences is recalling CD11b APC diagnostic reagent vials that may produce dim fluorescence signals, potentially causing false negative results and misdiagnosis of blood cancers.
Product
CD11b APC: ASR, REF: 340936, and CE, REF: 333143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0703-2024·2024-01-17
Diagnostic Test Kits for GI Panel May Return False Negatives Due to Manufacturing Issue
BioFire FILMARRAY GI Panel diagnostic test kits may return false negative results due to a manufacturing event, potentially leading to missed diagnoses and inappropriate treatment. The affected kits were distributed to locations in 16 U.S. states.
Product
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test intended for use with BIOFIRE FILMARRAY Systems.
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0644-2024·2024-01-17
Olympus ENDOEYE Videoscope Recalled for Reprocessing Instructions Deviations
Olympus Corporation recalls 1,403 ENDOEYE Flex endoscopic videoscopes due to deviations in reprocessing instructions. Affected devices may not be reprocessed properly for safe reuse in surgical procedures.
Product
OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0652-2024·2024-01-17
Abiomed Introducer Kit Sterile Barrier Compromise Due to Pouch Defect
Abiomed Introducer Kits may have holes in outer pouches that compromise sterility, exposing patients to bacterial contamination and risk of infection, bacteremia, or sepsis.
Product
Abiomed Kit, 14Fr Introducer, 13cm&25cm, Sterile Part of Pump Set (0048-0040, 0048-0045, 1000080)-Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3046
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0646-2024·2024-01-17
Medical Device Recall: Abiomed Axillary Insertion Introducer Sterile Barrier Breach
Abiomed Axillary Insertion Introducer Kits have holes in the outer pouch that may compromise sterility, potentially exposing patients to serious infections including bacteremia and sepsis.
Product
Abiomed Axillary Insertion Introducer -Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3006 Individual, and Part of Pump Set (005062, 0550-0008, 1000100, 0052-0011, 1000220)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0221-2024·2024-01-17
FDA Recalls Desloratadine Tablets Due to Manufacturing Defect
Lupin Pharmaceuticals is recalling Desloratadine 5mg tablets distributed nationwide because N-Nitroso impurity levels exceeded acceptable limits. Affected lots expire in January 2024.
Product
DESLORATADINE — DESLORATADINE (DESLORATADINE)
Category
Drug
Distribution
Distributed nationwide