Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

15476–15500 of 89774

HighFDA (Devices)·Z-0606-2024·2023-12-27
RAPIDPoint 500 Measurement Cartridges Recalled for Sodium Sensor Bias
Siemens is recalling RAPIDPoint 500 Systems Measurement Cartridges because the sodium sensor can develop a negative measurement bias that could delay diagnosis of serious electrolyte disorders or cause treatment errors.
Product
RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10844813
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0157-2024·2023-12-27
Nystatin Bulk Powder Recall for Incorrect Label Assay Value
Fagron, Inc. is recalling Nystatin 150 MU bulk powder for prescription compounding because the assay value on the label is incorrect.
Product
NYSTATIN 150 MU, Activity (as is): 6482 Units/mg, bulk powder container, Rx Only, For Prescription Compounding, Fagron, Inc. - 2400 Pilot Knob Rd. St Paul, MN 55120. NDC 51552-0041-1, Bar code 3 51552 00411 5
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-0607-2024·2023-12-27
RAPIDPoint 500 Diagnostic Cartridges Recall Due to Sodium Sensor Measurement Bias
Siemens is recalling RAPIDPoint 500 measurement cartridges because the sodium sensor can produce inaccurate readings, potentially leading to delayed diagnosis or incorrect treatment of electrolyte imbalances.
Product
RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491447
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0573-2024·2023-12-27
Injection Needles Recalled for Inadequate Manual Cleaning Process
Karl Storz is recalling 1,127 injection needles used in general and visceral surgery because the manual cleaning process cannot be adequately assured, potentially increasing infection risk for patients.
Product
Injection Needle, LUER-lock,0.8mm, REF: 26175PD
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0605-2024·2023-12-27
Venous probe connection cable defects in Cardiohelp-i extracorporeal support systems
Maquet Medical Systems USA is recalling venous probe connection cables for the Cardiohelp-i System due to insulation and wire breaks. Defective cables may prevent the system from receiving critical blood flow and temperature information.
Product
Venous probe connection cable (REF 701069333 and 701048804) used with the Cardiohelp-i System, part numbers 701072780 and 701041802
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0639-2024·2023-12-27
Vegan pumpkin pie products recalled due to foreign object contamination
Willamette Valley Pie Company is recalling vegan pumpkin pie products distributed in 12 states due to foreign object contamination. The voluntary recall was initiated in November 2023.
Product
Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan Pumpkin Pie WFM, BAKED BULK, 6 units/case. KEEP FROZEN - TRANSPORT AND STORE AT LESS THAN ZERO DEGREES F. Just Thaw and serve. Remove from freezer, removed plastic…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0607-2024·2023-12-27
Frozen vegetarian pizza recalled for undeclared wheat allergen
Shakespeare's Pizza Vegetarian Pizza is being recalled because it contains undeclared wheat, a common allergen. Affected products were distributed to retail stores in Missouri and Kansas and through online direct sales.
Product
Shakespeare's Pizza, Vegetarian Pizza, 25 oz, Keep Frozen; UPC 686 148 007 394; pack size 18 per case.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0574-2024·2023-12-27
Injection needles recalled due to cleaning efficacy concerns
Karl Storz Endoscopy is recalling injection needles used in general and visceral surgery due to concerns that the manual cleaning process cannot ensure adequate sterilization, which may increase infection risk.
Product
Injection Needle, single cvd. 70 degrees, REF: 738750; Injection Needle, single cvd. 80 degrees, REF: 738752; Injection Needle, bayonet, 13 cm, REF: 738756; Injection Needle, angular, 13 cm, REF: 738758; Needle, bayonet-shaped, REF: 810505; Needle, Septum, angular, REF: 810506
Category
Medical Device
Distribution
38 states
HighFDA (Food)·F-0604-2024·2023-12-27
Shakespeare's Pizza frozen pizza recalled for undeclared wheat
Shakespeare's Pizza is recalling 18,712 frozen pizzas due to undeclared wheat. The product was sold in retail stores in Missouri and Kansas and through online sales; consumers with wheat allergies should not consume it.
Product
Shakespeare's Pizza, Extra Cheese Pizza, 25 oz, Keep Frozen; UPC 686 148 007 370; pack size 20 per case.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0577-2024·2023-12-27
AcuMatch Hip System Recalled for Loss of Vacuum Integrity
Exactech is recalling AcuMatch Hip System devices due to loss of vacuum in the inner-most vacuum bag, with 3 complaints reported affecting 4 devices. Vacuum loss could compromise device packaging integrity.
Product
AcuMatch Hip System, Catalog Number 142-32-27
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0572-2024·2023-12-27
Injection needles and cannulas recalled for cleaning process efficacy issues
Karl Storz Endoscopy is recalling injection needles and cannulas because the manual cleaning process may not effectively remove contaminants, potentially exposing patients to infection risk.
Product
Injection Needle, 3 Fr., REF: 27030N; Injection Cannula, 6 Fr., REF: 27182A
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0588-2024·2023-12-27
Exactech Vantage Mobile Bearing Tibial Inserts Recalled Due to Vacuum Loss
Exactech is recalling Vantage Mobile Bearing Tibial Inserts due to loss of vacuum in the innermost vacuum bag. Three complaints involving four devices have been reported.
Product
Exactech Vantage Mobile Bearing Tibial Inserts, Catalog Numbers: a) 350-41-23, b) 350-42-03
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0584-2024·2023-12-27
Exactech Optetrak Logic PS Knee System Vacuum Loss Recall
Exactech is recalling certain Optetrak Logic PS Knee Systems due to potential loss of vacuum in the inner-most vacuum bag. The company has received 3 complaints involving 4 devices.
Product
Exactech Optetrak Logic PS Knee System, Catalog Numbers: 02-012-35-5009
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0580-2024·2023-12-27
Exactech Equinoxe Shoulder System recalled for loss of vacuum
Exactech is recalling specific models of its Equinoxe Shoulder System implants due to loss of vacuum in the inner-most vacuum bag. Four devices have been affected according to three complaints received.
Product
Exactech Equinoxe Shoulder System, Catalog Numbers: a) 314-23-02, b) 314-23-03, c) 314-23-13, d) 314-23-14, e) 314-23-15, f) 314-24-22, g) 314-24-23, h) 314-24-24, i) 314-24-32, j) 314-24-33, k) 314-24-34, l) 314-24-35
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0571-2024·2023-12-27
Injection Needle Recall Due to Cleaning Process Concerns
Karl Storz Endoscopy is recalling injection needles used in general and visceral surgery because the manual cleaning process cannot be assured effective, which may expose patients to a higher risk of infection.
Product
Injection Needle, REF: 25207
Category
Medical Device
Distribution
38 states
HighFDA (Food)·F-0605-2024·2023-12-27
Frozen pizza recalled for undeclared wheat allergen
Shakespeare's Pizza recalls Four Cheese Pizza due to undeclared wheat allergen. The product was distributed in Missouri, Kansas, and through online sales.
Product
Shakespeare's Pizza, Four Cheese Pizza, 25 oz, Keep Frozen; UPC 686 148 000 050; pack size 20 per case.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0582-2024·2023-12-27
Exactech Optetrak Knee Implant System Recalled for Vacuum Seal Failure
Exactech is recalling specific catalog numbers of the Optetrak Knee Implant System due to loss of vacuum in the protective inner bag. Three complaints affecting four devices have been reported.
Product
Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d) 200-02-35, e) 200-02-38, f) 200-02-41, g) 200-03-32, h) 200-07-29, i) 200-07-32, j) 200-07-35, k) 204-21-13, l) 204-22-26, m) 208-23-18, n) 208-24-13
Category
Medical Device
Distribution
16 states
HighFDA (Food)·F-0640-2024·2023-12-27
Candy Shop Rainbow Belts recalled for undeclared gluten in gluten-free product
Island Snacks, Inc. is recalling The Candy Shop Rainbow Belts because the product is labeled gluten-free but contains modified wheat flour. This poses a risk to consumers with celiac disease or gluten sensitivity.
Product
The Candy Shop Rainbow Belts Net Wt. 10.5 oz. (298g) SKU Code: 400255786276
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0578-2024·2023-12-27
Hip Implant Liner Recalled Due to Loss of Vacuum in Inner Bag
Exactech has recalled certain Alteon Hip XLE Liner hip implant components due to vacuum loss in the inner vacuum bag. The company has received 3 complaints involving 4 devices related to this issue.
Product
Exactech Alteon Hip XLE Liner, Catalog Numbers: a) 01-030-40-0636, b) 01-030-40-0640, c) 01-030-42-0536
Category
Medical Device
Distribution
16 states
SevereNHTSA·23V900000·2023-12-26
Volvo Recalls One 2020 VNL Truck for Steering Gear Assembly Defect
Volvo Trucks North America is recalling one 2020 VNL truck because the steering gear assembly may have been assembled with fewer recirculating balls than required, potentially causing a loss of steering control.
Product
VOLVO — VOLVO VNL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V899000·2023-12-26
2024 Mack Commercial Trucks Steering Gear Assembly Defect Recall
Mack is recalling approximately 284 certain 2024 Pinnacle, Anthem, and Terrapro commercial trucks with incorrectly assembled steering gear assemblies that could cause loss of steering control and increase crash risk. Dealers will inspect and replace defective gears free of charge.
Product
MACK — MACK ANTHEM (AN), PINNACLE (PI/PN), TERRAPRO (TE)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V901000·2023-12-26
2024 Hyundai Kona: Battery Cable Chafing May Cause Engine Fire
Hyundai is recalling 2024 Kona vehicles because battery cables may chafe and short circuit, increasing the risk of engine compartment fire. Dealers will install protective sheathing at no cost.
Product
HYUNDAI — HYUNDAI KONA
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·064-2023·2023-12-22
Scanga Meat Company Recalls Ground Beef Due to E. Coli O103
Scanga Meat Company is recalling approximately 563 pounds of ground beef products sold in Colorado due to possible E. coli O103 contamination.
Product
Scanga Meat Company — Scanga Meat Company Recalls Ground Beef Products Due to Possible E. Coli O103 Contamination
Category
Food
Distribution
1 state
SevereNHTSA·23V887000·2023-12-22
Mack Trucks Recalls 2024 Granite Vehicles for Steering Knuckle Defect
Mack Trucks is recalling 2024 Granite vehicles because bearing journals may not be fully seated in the steering knuckle assembly, which can lead to axle spindle fracture and increased crash risk.
Product
MACK — MACK GRANITE (GR)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V905000·2023-12-22
Ford vehicles recalled for oil pump belt failure and power braking loss
Certain 2016-2018 Ford Focus and 2018-2022 Ford EcoSport vehicles may have faulty oil pump drive belts or tensioners that can fail, causing engine stall and loss of power braking assist, increasing crash risk.
Product
FORD — FORD ECOSPORT, FOCUS
Category
Vehicle
Distribution
Distributed nationwide

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15476–15500 of 89774