State
73,388 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.
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 1,590 (28%) are Severe.
Which agencies issued them
These figures cover only the 5,590 recalls whose distribution notice names Iowa specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fudgeamentals LLC is recalling Peanut Butter Chocolate Fudge Bars (8 oz.) due to Salmonella contamination in the peanut butter ingredient. 189,096 units were affected nationwide.
Fudgeamentals LLC is recalling PEANUT BUTTER CHOCOLATE FUDGE BITES nationwide due to Salmonella contamination in the peanut butter ingredient. The recall affects 189,096 units.
Fudgeamentals Variety Tray (16 oz) is being recalled nationwide due to Salmonella contamination in its peanut butter component. Consumers should not consume the product and should discard it.
Fudgeamentals is recalling Peanut Butter Fudge Bites nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should not consume the affected product.
Forest River Aurora travel trailers (2021-2022) have a brake system defect where the breakaway switch may be incorrectly wired, preventing trailer brakes from activating. Dealers will provide free inspection and repairs.
Fudgeamentals LLC is recalling Tiger Butter Fudge Bar (8 oz) nationwide due to Salmonella contamination in the peanut butter ingredient. Affected lot codes: 22059007, 22083006, 22089006, 22130394.
Fudgeamentals LLC is recalling Marketside and Walmart Fudge Trio Holiday Fudge Trays nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should discard these products and not consume them.
Cummins is recalling 2020-2022 C500D6Re trailer-mounted generator sets because a logic error may prevent them from shutting down, posing burn and shock risks.
Haemonetics' TEG5000 Analyzer displays incorrect PlateletMapping assay values when connected to TEG Manager Software versions 1.1–4.3.1, potentially affecting laboratory test interpretation.
Akorn, Inc. is recalling 44,400 bottles of Fluticasone Propionate Nasal Spray nationwide due to a defective container that prevents proper dispensing. Patients should contact their healthcare provider or pharmacist.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles (5.25 oz) due to milk contamination. The recall affects 6,400 units distributed nationwide and internationally.
One lot of DVR Anatomic distal radius orthopedic plates was incorrectly etched during manufacturing and may have been placed into kits labeled as a different plate model. The affected plates were distributed to healthcare facilities nationwide.
Cummins is recalling PD7000 Electric Drivetrains because an improperly grounded air compressor can cause electric shock. Owners will receive a free repair to install a ground strap.
GE Healthcare is recalling backup batteries in Avance CS2 and CS2 Pro anesthesia machines manufactured after April 1, 2019. Batteries may fail earlier than expected, affecting approximately 6,600 devices worldwide.
Skytron recalls its GCX Channel Mounting Accessory (model H8-300-40-A) because mounting screws may loosen or pull out when used as a monitor mount on surgical booms. Affected units were distributed worldwide.
Daytrana (methylphenidate) patches are being recalled due to ripping patches and poor adhesive transfer affecting drug delivery. This Class II recall involves 8,559 cartons distributed nationwide.
PD-Rx Pharmaceuticals recalled Losartan Potassium 50 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. The recall affects 687 bottles across multiple lots.
Davol HydroSurg Plus Laparoscopic Irrigators cannot provide irrigation. The FDA issued a Class II recall affecting 4,780 units worldwide.
ROi CPS LLC is recalling 180 CV Minor Kit units due to a nonsterile component accidentally packaged in the sterile kit, posing a contamination and infection risk.
The QMS Tacrolimus Calibrator Set is recalled because calibrators recovered 82-94% of target values, causing inaccurate (over-quantitated) patient drug test results. This affects healthcare facilities in 20 US states and 9 countries.
The ProudP Everyday Uroflow Tracker app may record lower-than-actual urination measurements when a hearing aid or AirPods Live Listen feature is active on the same iPhone, due to interference with the app's sound-based measurement system.
C.R. Bard is recalling 457 Sensica Urine Output System units nationwide due to complaints about urine output measurement accuracy.
Arrow International is recalling the Arrow Three-Lumen CVC due to incorrect gravity flow rates on the product lidstock. The defect may affect fluid and medication delivery through the catheter.
PD-Rx Pharmaceuticals recalls Losartan Potassium Tablets (25 mg, 90-tablet bottles) due to Current Good Manufacturing Practice deviations. Specific lot numbers contain AZIDO impurity levels above acceptable limits.
PD-Rx Pharmaceuticals is recalling Losartan Potassium 100 mg tablets due to AZIDO impurity levels above acceptable limits detected during manufacturing. Approximately 1,320 bottles were distributed nationwide.