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 deaths or serious injuries are reported, 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

12951–12975 of 27721

HighFDA (Devices)·Z-1690-2024·2024-05-01
Philips Patient Information Center iX UPS devices recalled for potential power failure
Philips is recalling certain Patient Information Center iX Uninterruptable Power Supply devices due to potential power supply failures that could cause the monitoring system to shut down, risking delays in detecting patient condition changes.
Product
Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporation) 120V Uninterruptable Power Supply Model: SCL500RM1U 2. APC (Schneider Electric IT Corporation) 230V Uninterruptable Power Supply Model: SCL500R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1599-2024·2024-05-01
ACUSON Juniper ultrasound systems display incorrect cardiac measurements
Siemens ACUSON Juniper ultrasound systems may display the wrong cardiac measurement value when configured to show minimum or maximum values, potentially leading to misdiagnosis.
Product
ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System, REF: 11653093, running software version VA10x with DICOM SR Cardiac option, from VB10A to VB10G, VB11A, VB11B, VB30B and VB30C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1602-2024·2024-05-01
Abbott Alinity m System camera generates error with certain tubes
Abbott Molecular is recalling 1,012 Alinity m System units due to a camera detection issue that generates an error message when certain third-party transport medium tubes lack a sample rack retention bar.
Product
Alinity m System, Part Number: 08N53-002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1617-2024·2024-05-01
Biomet OrthoPak Bone Growth Stimulator System Recalled Due to Lead Wire Damage
The Biomet OrthoPak Bone Growth Stimulator System is being recalled due to potential lead wire sheath damage that could prevent therapeutic signal delivery and delay patient treatment nationwide.
Product
Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. Part Number: 1067718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1626-2024·2024-05-01
Hip implant acetabular shell deburring defect triggers manufacturer recall
The TRIDENTII HEMI CLUSTER58F hip implant acetabular shell may have excessive deburring creating a smooth edge. Howmedica Osteonics Corp. is recalling affected units.
Product
TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0464-2024·2024-05-01
FDA Recalls Fluorescein Sodium Ophthalmic Strips for Manufacturing Defect
The FDA is recalling FUL-GLO Fluorescein Sodium Sterile Ophthalmic Strips (4,648 cartons) nationwide due to unspecified impurities in the active ingredient exceeding USP standards.
Product
FUL-GLO, Fluorescein Sodium Sterile Ophthalmic Strips USP (0.6 mg Fluorescein), 300 sterile strips per carton, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-403-03.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1604-2024·2024-05-01
Redux Electrolyte Creme Recalled for Low Viscosity Defect
Parker Laboratories is recalling Redux Electrolyte Creme, a highly conductive medical electrolyte product, due to demonstrated low viscosity.
Product
Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1625-2024·2024-05-01
TRIDENTII HEMI Hip Implant Acetabular Shell Deburring Defect Recall
Howmedica Osteonics is recalling the TRIDENTII HEMI CLUSTER54E hip implant due to excessive deburring on the acetabular shell edge that may affect implant performance. The recall involves 225 units distributed nationwide and internationally.
Product
TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0590-2024·2024-05-01
Tissue Processor Recall: HistoCore PEGASUS May Produce Damaged Specimens
Leica is recalling 98 HistoCore PEGASUS automated tissue processors due to a protocol configuration error that can produce poorly processed or damaged biopsy specimens.
Product
Leica HistoCore PEGASUS (PROCESSOR, TISSUE, AUTOMATED)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1629-2024·2024-05-01
Hip replacement acetabular shell recalled for excessive deburring
Howmedica Osteonics is recalling TRIDENTII PSL CLUSTER50D acetabular shells for hip replacements due to excessive deburring resulting in smooth edges on the shell.
Product
TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1618-2024·2024-05-01
Replacement Lead Wires Recalled for Risk of Treatment Delivery Failure
EBI, LLC recalls 829 replacement lead wire assemblies (Part 1067724-2) distributed nationwide since May 1, 2023. Damaged wire sheaths may prevent therapeutic treatment signals from reaching electrodes, potentially delaying treatment.
Product
20" Lead Wires, Replacement Part Number: 1067724-2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0472-2024·2024-05-01
Prescription Drug Recall: Diltiazem Extended-Release Capsules Fail Dissolution Test
Glenmark Pharmaceuticals is recalling 3,264 bottles of Diltiazem Hydrochloride Extended-Release Capsules nationwide due to failure to meet dissolution specifications. The affected lot may not release the medication properly in the body.
Product
DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0474-2024·2024-05-01
Minocycline Extended-Release Tablets Recalled for Manufacturing Quality Control Failure
EPI Health is recalling minolira extended-release tablets due to manufacturer discontinuation of quality control programs affecting product identity, strength, and purity. The recall covers 12,808 bottles distributed nationwide.
Product
minolira (minocycline hydrochloride) extended-release tablets, 105mg 30-count Bottle, Rx Only, Mfg by: Dr Reddy's Laboratories Limited, INDIA, Manufactured for: EPI Health, LLC, Charleston, SC 29403, NDC 71403-101-30.
Category
Drug
Distribution
Distributed nationwide
HighCPSC·24208·2024-04-25
Oregon Tool Recalls Log Splitters Due to Injury Hazards
Oregon Tool is recalling about 29,560 log splitters and cylinder kits because the hydraulic cylinder rod can separate from the piston, causing unexpected movement of the wedge that poses injury risks. No injuries have been reported.
Product
Oregon, PowerPro, Country Tuff, and Speeco branded log splitters and cylinder kits
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24210·2024-04-25
JAKKS Pacific Recalls Mario Kart 24V Ride-On Racer Cars Due to Crash Hazard
JAKKS Pacific is recalling certain Mario Kart 24V Ride-On Racer Cars because the acceleration pedal can become clogged with debris and stick, causing the vehicle to crash. The company has received 65 reports of clogged pedals, including 15 crashes with one minor injury.
Product
Mario Kart™ 24V Ride-On Racer Cars
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24211·2024-04-25
Kids' Bike Helmets Recalled for Failure to Meet Safety Standards
Chau River Sports Outdoors is recalling about 200 kids' bike helmets sold on Temu.com because they fail to meet federal safety requirements and may not protect children's heads in a crash.
Product
Kid's Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24212·2024-04-25
Crosman Icon Air Rifles Recalled Due to Unexpected Discharge Injury Hazard
Crosman is recalling about 2,500 Icon Air Rifles because an uncocked and loaded rifle can discharge unexpectedly if jolted or dropped, posing an injury hazard. One unintended discharge has been reported, though no injuries have occurred.
Product
Crosman Icon Air Rifles
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1163-2024·2024-04-24
Brazil Seed Dietary Supplement Recalled for Yellow Oleander Contamination
HandNatural recalls H&Natural Brazil Seed supplement due to presence of yellow oleander and its components. The product was distributed via internet sales.
Product
H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOTTLE, 2 BLACK BOTTLES.
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-1160-2024·2024-04-24
Tejocote Root Dietary Supplement Recalled Due to Yellow Oleander
H&Natural is recalling tejocote root supplement due to the presence of yellow oleander and its components. The product was distributed exclusively through internet sales.
Product
H&NATURAL TEJOCOTE ROOT TWO PACK 180 PIECES, 6 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1158-2024·2024-04-24
H&Natural Tejocote Root Dietary Supplement Recalled Due to Yellow Oleander
HandNatural is recalling H&Natural Tejocote Root dietary supplement because the product contains yellow oleander and its components, which pose a health risk.
Product
H&NATURAL TEJOCOTE ROOT Dietary Supplement Net WT 0.36 oz (10g)
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1397-2024·2024-04-24
Elekta Disposable Biopsy Needles Recalled for Microscopic Internal Debris
Elekta recalled disposable biopsy needles from batch 837838839 that may contain microscopic stainless steel debris inside. The sterility of the needles has not been affected, and this issue has been reported from only one site.
Product
Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, 2.1mm Diameter / 14 Gauge, containing 6 inner boxes labeled REF 911761, Disposable Biopsy Needle Kit for Leksell Stereotactic System. Each inner box of REF 911761 contains a Tyvek bag labeled REF 91
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1166-2024·2024-04-24
H&Natural Brazil Seed dietary supplement recalled for yellow oleander
HandNatural is recalling H&Natural Brazil Seed 30-piece supplements due to the presence of yellow oleander and its components in the product. Consumers should stop using the product immediately and dispose of it safely.
Product
H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, BLACK BOTTLE
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1159-2024·2024-04-24
HandNatural Brazil Seeds Recalled for Toxic Yellow Oleander Contamination
HandNatural Brazil seeds (5g) have been recalled for contamination with yellow oleander, a highly toxic substance. FDA classified this as a Class I recall due to serious health hazards.
Product
Brazil Seed Net WT 0.18 oz (5g)
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1167-2024·2024-04-24
H&Natural Brazil Seed supplement recalled for yellow oleander contamination
H&Natural Brazil Seed is a botanical supplement sold online that is being recalled because the product contains yellow oleander and its components. The manufacturer is HandNatural.
Product
H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, YELLOW BOTTLE.
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1170-2024·2024-04-24
Brazil seed dietary supplement recalled due to yellow oleander contamination
HandNatural Brazil seed supplement recalled for containing yellow oleander, a toxic plant. Affected products sold online with expiration dates 05/24 and 03/24.
Product
H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 BLACK BOXES.
Category
Food
Distribution
0 states

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12951–12975 of 27721