State

Iowa product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24776–24800 of 79102

ModerateFDA (Drugs)·D-0076-2022·2021-11-03
Xpect First Aid Extra Strength Pain Away tablets recalled for failed stability specifications
Ultra Seal Corporation is recalling Xpect First Aid Extra Strength Pain Away tablets nationwide due to out-of-specification results for Salicylic Acid, a compound related to Aspirin, indicating failed stability testing.
Product
Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/package, Packaged in 12,000 Packets/Case, Material# 111519, Mfg. for: Cintas First Aid & Safety, Mason, OH 45040 (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0075-2022·2021-11-03
Advance Formula Pain Reliever tablets recalled for failed stability specifications
Ultra Seal Corporation is recalling Advance Formula Pain Reliever tablets (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) distributed nationwide due to out-of-specification results for Salicylic Acid, an Aspirin-related compound.
Product
Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets Per Packet, Packaged in 12,000 Packets/Case, PO# 007564-00, Item# 1170, Mfg. for: Advanced First Aid, Baltimore, MD 21237; American Safety & First Aid, Osceola, IN 46561…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0074-2022·2021-11-03
North by Honeywell Pain Stopper Extra Strength tablets recalled for failed stability
Ultra Seal Corporation is recalling North by Honeywell Pain Stopper Extra Strength tablets nationwide because stability testing found out-of-specification results for Salicylic Acid, an aspirin-related compound.
Product
North by Honeywell PAIN STOPPER EXTRA STRENGTH (Acetaminophen 250 mg, Aspirin 250 mg, Caffeine 65 mg) tablets, 2 tablets per packet, Packaged in 5,000 Packets/Case, PO# B121242, Item# 853500-01, Dist. By Honeywell Safety Products USA, Smithfield, RI 02917
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0168-2022·2021-11-03
GORE CARDIOFORM Septal Occluder Labeled with Incorrect Expiration Date
W L Gore & Associates is recalling GORE CARDIOFORM Septal Occluder devices labeled with a 3-year expiration date instead of the correct 2-year date. Mislabeling could result in use of devices beyond their intended safe lifespan.
Product
REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617647 *Not distributed within the US
Category
Medical Device
Distribution
47 states
ModerateFDA (Drugs)·D-0073-2022·2021-11-03
AERO Tab Pain Reliever Tablets Recalled for Failed Stability Specifications
Ultra Seal Corporation is recalling AERO Tab Pain Reliever tablets nationwide because out-of-specification results were found for Salicylic Acid, an Aspirin-related compound, indicating failed stability testing.
Product
AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets Per Packet, Packaged in 10,000 Packets/Case, PO# 11938, Mfg. for: Aero Healthcare, Valley Cottage, NY 10989 (Shipping Label )
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2022·2021-11-03
Loratadine-D Extended-Release Tablets Recalled for Failed Moisture Limits
Sun Pharmaceutical Industries is recalling 22,752 blister packs of Loratadine-D Extended-Release Tablets (10mg/240mg) distributed nationwide due to failed moisture limits. The affected lot is AC14635 with expiration date 12/2022.
Product
LORATADINE AND PSEUDOEPHEDRINE SULFATE — LORATADINE AND PSEUDOEPHEDRINE SULFATE (LORATADINE AND PSEUDOEPHEDRINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0070-2022·2021-11-03
PainAway II Acetaminophen/Aspirin/Caffeine Tablets Recalled for Failed Stability
Ultra Seal Corporation is recalling PainAway II tablets nationwide due to failed stability specifications. Testing found out-of-specification levels of Salicylic Acid, an aspirin-related compound.
Product
PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets/pk, packaged in 12,000 Packets/Case, Material # 11161, Mfg. for Respond Industries First Aid, Mason, OH 45040 (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0166-2022·2021-11-03
GORE CARDIOFORM Septal Occluders Recalled for Incorrect Expiration Date
W. L. Gore & Associates is recalling GORE CARDIOFORM Septal Occluders labeled with incorrect 3-year expiration dates instead of 2-year dates. This labeling error affects devices distributed across the United States and internationally.
Product
REF/Catalogue Number GSX0025A, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631025 *Not distributed within the US
Category
Medical Device
Distribution
47 states
ModerateFDA (Devices)·Z-0167-2022·2021-11-03
GORE CARDIOFORM SEPTAL OCCLUDER Recalled for Incorrect Expiration Date Labeling
GORE CARDIOFORM SEPTAL OCCLUDER devices are recalled for labeling errors: 95 units marked with 3-year expiration instead of correct 2-year date. Affected units distributed across US and international locations.
Product
REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617630 *Not distributed within the US
Category
Medical Device
Distribution
47 states
LowFDA (Drugs)·D-0072-2022·2021-11-03
ZEE+ Painaid ESF Tablets Recalled for Failed Stability Specifications
Ultra Seal Corporation is recalling ZEE+ Painaid ESF Extra-Strength Formula tablets nationwide due to out-of-specification results for Salicylic Acid, an aspirin-related compound. The recall affects 50-count and 125-count packages with lot numbers AK-9547 (exp. April 22) and AK-9941 (exp. December 22).
Product
ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Packaged in a) 50-count packages/carton, b) 125-count packages/carton, PA-ESF 1414Z, Dist. by: Zee Medical Distributors, LLC Mason, OH 45040…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0080-2022·2021-11-03
Rizatriptan Benzoate Orally Disintegrating Tablets Recalled for Out-of-Specification Impurities
Macleods Pharma USA is recalling Rizatriptan Benzoate 10mg orally disintegrating tablets nationwide due to out-of-specification results in organic impurities testing of controlled samples.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0069-2022·2021-11-03
Kirkland Signature AllerClear D 24 HR Tablets Recalled for Moisture Failure
SUN PHARMACEUTICAL INDUSTRIES INC is recalling Kirkland Signature AllerClear D 24 HR (Loratadine and Pseudoephedrine Sulfate) tablets nationwide because the product failed to meet moisture content limits.
Product
KIRKLAND SIGNATURE ALLERCLEAR D 24 HR — KIRKLAND SIGNATURE ALLERCLEAR D 24 HR (LORATADINE AND PSEUDOEPHEDRINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0071-2022·2021-11-03
Vica-Cet Back Pain Relief tablets recalled for stability specification failure
Ultra Seal Corporation is recalling Vica-Cet Back Pain Relief tablets nationwide because certain lots failed stability testing and contain out-of-specification levels of Salicylic Acid, an aspirin-related compound.
Product
Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000 packets, PO# 8967, Mfg. for Tellus/The Provision First Aid Line (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V850000·2021-11-02
Thomas Built Buses Recalling 2020-2022 Models for Alternator Fire Risk
Daimler Trucks is recalling 1,434 Thomas Built school buses because a loose alternator cable connection may cause electrical arcing and increase the risk of a fire.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V848000·2021-11-02
Alfa Romeo Giulia Recalled for Tires with Incorrect Load Rating
FCA US is recalling 2020 Alfa Romeo Giulia vehicles because some may have tires with a lower load rating than intended, increasing crash risk.
Product
ALFA ROMEO — ALFA ROMEO GIULIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V851000·2021-11-02
Oshkosh Recalls 2020-2021 S-Series Vehicles for Power Steering Defect
Oshkosh is recalling 2020-2021 S-Series vehicles because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of steering assist.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V849000·2021-11-01
Heartland Cyclone and Road Warrior RVs recalled for loose electrical wires
Heartland Recreational Vehicles is recalling 2019-2021 Road Warrior and 2020-2021 Cyclone trailers because wire securement lugs may be improperly tightened. Loose wires can cause electrical arcing and increase fire risk.
Product
HEARTLAND — HEARTLAND CYCLONE, ROAD WARRIOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V844000·2021-10-29
Kia Recalls 2017-2018 Optima Hybrid Vehicles for Engine Bearing Wear
Kia is recalling 2017-2018 Optima Hybrid and Plug-In Hybrid vehicles because premature engine bearing wear can cause engine damage, increasing the risk of fire or a crash.
Product
KIA — KIA OPTIMA HYBRID, OPTIMA PHEV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E092000·2021-10-29
Windshield Fastener Recall: Axalta Coating Systems Bonding Defect
Axalta Coating Systems is recalling windshields that may not be adequately bonded to Ford and Chrysler vehicles due to a coating defect.
Product
VISIBILITY:WINDSHIELD:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V843000·2021-10-29
Mercedes-Benz Recalls 2021 S 580 for Engine Stall Risk
Mercedes-Benz is recalling 2021 S 580 and Maybach S 580 vehicles because a software error may cause the engine to stall without restarting, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ S 580
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V845000·2021-10-29
Thor Motor Coach Recalls 2017 Outlaw, Challenger, and Miramar Motorhomes
Thor Motor Coach is recalling 2017 Outlaw, Challenger, and Miramar motorhomes because external compartment door skins may separate during transit, creating a road hazard.
Product
THOR MOTOR COACH — THOR MOTOR COACH CHALLENGER, MIRAMAR, OUTLAW
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-10292021·2021-10-29
USDA Issues Public Health Alert for Citterio Salame Sticks Due to Salmonella
USDA FSIS issued a public health alert for Citterio Premium Italian-Style Salame Sticks due to possible Salmonella contamination linked to a multistate outbreak.
Product
FSIS Issues Public Health Alert for Salame Stick Products Due to Possible Salmonella Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V846000·2021-10-29
Tesla Model 3 Forward Collision Avoidance System Software Error
Tesla is recalling certain 2017-2021 Model 3, S, X, and Y vehicles due to a software error that may cause false forward-collision warnings or unexpected automatic emergency brake activation. No injuries have been reported.
Product
TESLA — TESLA MODEL S, MODEL X, MODEL 3, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V842000·2021-10-28
2021 Dodge Durango Rear Spoiler May Detach, Becoming Road Hazard
Chrysler is recalling 2021 Dodge Durango vehicles because the rear spoiler may not be properly aligned and could detach during liftgate use, creating a road hazard. Dealers will replace the spoiler free of charge.
Product
DODGE — DODGE DURANGO
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22704·2021-10-28
Design Within Reach Arc Collection Furniture Recalled for Excess Lead Paint
Design Within Reach is recalling its Arc Collection furniture (chairs, tables, and barstools) because the surface paint contains lead levels exceeding the federal lead paint ban, posing a risk of lead poisoning to young children.
Product
Arc Collection Furniture
Category
Consumer Product
Distribution
Distributed nationwide