State

Iowa product recalls

73,584 recalls have nationwide distribution and so reach Iowa. 5,593 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total: 5,593
Critical: 910
Severe: 1,591
Most recent: 2026-10-24

Of the 5,593 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 1,591 (28%) are Severe.

Which agencies issued them

These figures cover only the 5,593 recalls whose distribution notice names Iowa specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

701–725 of 79177

SevereFDA (Drugs)·D-0810-2026·2026-09-09
Baxter Recalls Dexmedetomidine Hydrochloride Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Dexmedetomidine Hydrochloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0821-2026·2026-09-09
Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Daptomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall covers the US, Puerto Rico, and Chile.
Product
Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3084-2026·2026-09-09
Fresenius Medical Care Recalls 5008X Standard HD Pre-Flush Blood Tubing Sets
Fresenius Medical Care is recalling 120 units of 5008X Standard HD Pre-Flush Blood Tubing Sets due to a heightened probability of blood leaks during treatment.
Product
5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3062-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 18,290 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26E063000·2026-09-09
Ford Recalls Battery Energy Control Modules for Software Defect
Ford is recalling specific Battery Energy Control Modules (BECM) because software errors may cause incorrect charge readings or overheating, increasing crash and fire risks.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3048-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 104 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT, Model Number: ACC010741; 2) KIT ANESTHESIA L&D A- LINE SET, Model Number: DYKMBNDL199A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3057-2026·2026-09-09
Medline Blood Culture Kits Recalled for Potential Sterility Breach
Medline is recalling 3,650 blood culture kits nationwide due to potential packaging defects that may compromise sterility and expose patients to microbial contamination.
Product
Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0817-2026·2026-09-09
Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to CGMP deviations. The affected product was distributed in the US, Puerto Rico, and Chile.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V583000·2026-09-09
Daimler Trucks Recalls Freightliner and Western Star Trucks for Brake Defect
Daimler Trucks North America is recalling certain 2020-2023 Freightliner Cascadia and 2022 Western Star 49X trucks because corroded brake valves may cause the vehicle to pull during braking.
Product
FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 49X
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0820-2026·2026-09-09
Baxter Recalls Vancomycin Injection Due to CGMP Deviations
Baxter Healthcare is voluntarily recalling specific lots of Vancomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3060-2026·2026-09-09
Medline C-Section Prep Kits Recalled for Potential Sterility Breach
Medline is recalling 352 C-Section Prep kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) C-SECTION PREP, Model Number: DYNJ32702B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0814-2026·2026-09-09
Baxter Recalls Nexterone Amiodarone Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Nexterone (amiodarone hydrochloride) injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
NEXTERONE — NEXTERONE (AMIODARONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V578000·2026-09-09
Ford Recalls 2023-2027 F-150 Trucks for Fuel Tank Securing Defect
Ford is recalling 2023-2027 F-150 vehicles because the fuel tank may be improperly secured, posing risks of fuel leaks, engine stalls, or the tank detaching while driving.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0847-2026·2026-09-09
Golden State Medical Supply Recalls Prasugrel Tablets for Failed Dissolution
Golden State Medical Supply is recalling 6,791 bottles of 10mg Prasugrel tablets because the product failed dissolution specifications.
Product
PRASUGREL — PRASUGREL (PRASUGREL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3053-2026·2026-09-09
Medline Ultrasound Breast Pack Recalled for Potential Sterility Breach
Medline is recalling 300 Ultrasound Breast Packs due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) ULTRASOUND BREAST PACK, Model Number: DYNJ63375C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0808-2026·2026-09-09
Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0834-2026·2026-09-09
Teva Recalls Trazodone Hydrochloride Tablets Due to Foreign Material
Teva Pharmaceuticals is recalling 175,392 bottles of Trazodone Hydrochloride 50 mg tablets because they may contain foreign tablets or capsules.
Product
TRAZODONE HYDROCHLORIDE — TRAZODONE HYDROCHLORIDE (TRAZODONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V582000·2026-09-09
Ford Recalls 2023-2025 Mustang Mach E for Battery Software Defect
Ford is recalling 2023-2025 Mustang Mach E vehicles with specific battery modules due to software errors that may cause power loss or fire.
Product
FORD — FORD MUSTANG MACH E
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3087-2026·2026-09-09
Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk
Fresenius Medical Care is recalling 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.
Product
5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0807-2026·2026-09-09
Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling Daptomycin in Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg per 50 mL (10 mg/mL), 500 mg total, in 50 mL Single Dose Container (24 bags/carton), Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0714-24.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26V577000·2026-09-09
Ford Recalls 2026 F-150 Trucks Due to Improperly Tightened Stabilizer Rod Fasteners
Ford is recalling 2026 F-150 vehicles because stabilizer rod fasteners may not be tightened properly, which can cause the rod to shift and increase crash risk.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3046-2026·2026-09-09
AVID Medical Recalls Halyard Neurological Sponges Due to Endotoxin Variability
AVID Medical is recalling specific lots of Halyard medical convenience kits containing Ritmed Neurological Sponges due to potential endotoxin level variability.
Product
Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960, Model/Item Number (kit) ANPP15-01; 3) ANEURYSM PACK, Model/Item Number (kit) BPAY14-01; 4) SPINE PACK, Model/Item Number (kit) HSLM53-01…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V580000·2026-09-09
Ford Recalls 2026 Bronco Vehicles Due to Air Bag Mounting Defect
Ford is recalling 2026 Bronco vehicles because a metal burr on the side curtain air bag bracket may tear the bag during deployment, increasing injury risk.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0805-2026·2026-09-09
Baxter Recalls Vancomycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Vancomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3059-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 3,752 Labor CDS and Vag Delivery Admission Bags due to packaging wrinkles that may compromise sterility, risking microbial contamination.
Product
Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F
Category
Medical Device
Distribution
Distributed nationwide