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.

Agency

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926–950 of 26077

HighFDA (Devices)·Z-1872-2026·2026-04-29
AccuVu Angiographic Catheter recall due to manufacturing defect
Angiodynamics is recalling AccuVu Angiographic Catheters due to a manufacturing defect that may prevent a guidewire from passing through the catheter hub. The defect could interfere with proper device function during medical procedures.
Product
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box), H787137090050 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1941-2026·2026-04-29
Diversatek Viper Wire Guided Balloon Dilator Inflation Tag Incorrect
Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the attached inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.
Product
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 18mm-19mm-20mm, REF 1205-20
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-1922-2026·2026-04-29
Beckman Coulter Access Total T4 Calibrator Recalled for Inaccurate Results
Beckman Coulter is recalling Access Total T4 Calibrator lots because they produce falsely low patient results on DxI 600/800 instruments, potentially leading to unnecessary testing, delayed treatment for thyroid disorders, and incorrect dosing in pregnant patients.
Product
Access Total T4 Calibrator, Catalog No. 33805
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1866-2026·2026-04-29
Angiodynamics Soft-Vu Angiographic Catheter Guidewire Blockage Risk
Angiodynamics is recalling the Soft-Vu Angiographic Catheter, Kumpe, Non-Braided due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
Product
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1807-2026·2026-04-29
Ultraviolet-C Germicidal Wand Recalled for Unsafe UVC Radiation Exposure
Uvlizer handheld UV-C wands may expose users and bystanders to ultraviolet-C radiation levels above international safety limits during normal use, posing risk of skin and eye injury.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1916-2026·2026-04-29
MAC Two-Lumen Central Venous Access Kit Recalled Due to Manufacturing Defect
ARROW INTERNATIONAL is recalling the MAC Two-Lumen Central Venous Access Kit due to incorrect manufacturing of the liquid adhesive component. The recall affects 90 units distributed across nine U.S. states.
Product
MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous access and catheter introduction
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1894-2026·2026-04-29
LeadCare Plus Blood Lead Test Kit Recalled for Unexpectedly Elevated Results
Magellan Diagnostics is recalling LeadCare Plus Blood Lead Test Kits (Catalog Number 82-0004) because they may produce falsely elevated lead results when used with certain third-party micro-collection devices, potentially causing delayed testing and unnecessary follow-up testing.
Product
LeadCare¿ Plus Blood Lead Test Kit; Catalog Number: 82-0004; The LeadCare¿ Plus kit is provided with the following materials: " Sensors (4 containers of 24 each; 96 tests) " Treatment Reagent Tubes (4 packages of 24 each; 96 tests) " Calibration Button (1 @) " Lead Contro
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1929-2026·2026-04-29
LSL Healthcare Central Line Dressing Change Kit Recalled for Non-Sterility
LSL Healthcare is recalling its Standard Central Line Dressing Change Kit (Model 2717J) because the included Webcol Large Alcohol Prep Pads were found to be non-sterile.
Product
LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1871-2026·2026-04-29
Angiodynamics Soft-Vu Angiographic Catheter Kumpe Recall
Angiodynamics is recalling Soft-Vu Angiographic Catheter, Kumpe devices due to a manufacturing defect that may prevent guidewire passage through the catheter hub.
Product
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN No.: H787107343015 (Box), H787107343010 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2026·2026-04-29
AccuVu Angiographic Catheter, Omni Flush, Non-Braided Defect Recall
Angiodynamics recalls AccuVu Angiographic Catheters due to a manufacturing defect that may prevent guidewires from passing through the catheter hub. The affected devices were distributed worldwide.
Product
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1923-2026·2026-04-29
Oxoid Agglutinating Sera Salmonella 9-0 Serotyping Classification Error
Remel Europe Ltd. is recalling specific lots of Oxoid Agglutinating Sera, Salmonella 9-0 due to cross-reactivity that may misidentify Salmonella 9-O serotypes as 2-O serotypes in laboratory testing.
Product
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1907-2026·2026-04-29
OER-ELITE Endoscope Reprocessor Connecting Tubes Lock Failure Recall
Olympus Corporation of the Americas is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2119) due to potential premature failure of the Version 2 reprocessor connecting tube lock levers.
Product
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1913-2026·2026-04-29
Arrow Epidural Catheter Kits Recalled Due to Adhesive Manufacturing Defect
Arrow International is recalling FlexTip Plus Epidural Catheter and FlexBlock Continuous Peripheral Nerve Block Catheter Kits due to incorrect manufacturing of liquid adhesive. The recall affects 190 units distributed nationwide.
Product
FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural Catheter kit permits access to the epidural space for administration of epidural ane
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2026·2026-04-29
Soft-Vu Angiographic Catheter Cobra Non-Braided Manufacturing Defect
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided devices due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
Product
Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Product/UPN No.: H787107140175 (Box), H787107140170 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0674-2026·2026-04-29
FDA Recalls El Mexicano Instant Horchata Drink for Undeclared Milk
Marquez Brothers International is recalling EL MEXICANO Instant Horchata Drink due to undeclared milk. The product contains whey and lactose not declared on the label, posing a risk to consumers with milk allergies.
Product
EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190204 Item: 102279
Category
Food
Distribution
29 states
SevereCPSC·26435·2026-04-23
32 Degrees Heated Socks Recalled Due to Burn Hazard
32 Degrees Heated Socks sold at Costco from August 2025 to March 2026 are recalled due to burn hazard. When worn during high-intensity activities, the socks can cause first- or second-degree burns.
Product
32 Degrees Heated Socks
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26432·2026-04-23
Children's Tower Stools Recalled Due to Collapse and Entrapment Hazards
TOETOL tower stools can collapse or tip over while in use. Children's torsos can fit through side openings, creating entrapment risks. The firm received 18 collapse reports with 11 injuries.
Product
TOETOL Tower Stools
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26430·2026-04-23
Wiifo Children's Tower Stools Recalled for Collapse, Tip-Over, and Entrapment Hazards
Approximately 9,700 Wiifo Children's Tower Stools may collapse or tip over, with children's torsos able to fit through side openings, risking serious injury or death. The firm has reported 22 collapse incidents resulting in 6 injuries.
Product
Wiifo Children's Tower Stools
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26431·2026-04-23
Adjustable dumbbells recalled for dislodging weight plates causing injuries
About 50,000 FitRx SmartBell adjustable dumbbells are recalled because weight plates can dislodge during use. There have been at least 6 documented injuries including broken toes, bruises, contusions, and lacerations.
Product
FitRx SmartBell Quick-Select 5-52.5lbs Adjustable Dumbbells
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26436·2026-04-23
Magnetic Stick Figure Sets Recalled for Magnet Ingestion Risk
BlissfulDestiny Magnetic Stick Figure Sets sold on Walmart.com are recalled for loose magnets that pose an ingestion hazard to children, potentially causing intestinal injury or death.
Product
BlissfulDestiny Magnetic Stick Figure Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26434·2026-04-23
Autobrush Recalls Sonic Pro Kids Toothbrush Boxes Due to Battery Ingestion Risk
Autobrush is recalling about 48,000 Sonic Pro Kids toothbrush boxes sold online from March 2023 to December 2025. The packaging contains a coin cell battery children can easily access, posing a risk of serious injury or death if swallowed.
Product
Autobrush Sonic Pro Kids Toothbrush Boxes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26438·2026-04-23
Cpzzkq Baby Loungers Recalled for Suffocation Risk from Padding
Cpzzkq baby loungers sold on Amazon violate mandatory infant safety standards because padding can obstruct breathing, posing a suffocation risk. About 2,100 units were distributed; no injuries reported.
Product
Cpzzkq Baby Loungers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26433·2026-04-23
Children's Tower Stools Recalled for Tip-Over and Entrapment Hazards
AMZCMJ DGD children's tower stools can collapse or tip over while in use, allowing a child's torso to fit through side openings and become entrapped. Four injuries have been reported from seven incidents.
Product
AMZCMJ DGD Children's Tower Stools
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26437·2026-04-23
Baby Loungers Recalled Due to Fall, Suffocation, and Entrapment Hazards
HappyGira's baby loungers violate infant safety standards due to fall and suffocation hazards. About 70 units sold online from September 2025 to February 2026 are affected.
Product
Sweetie Baby and Style Life Eleven Baby Loungers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26429·2026-04-23
mGanna Sodium Hydroxide Pellet Bags Recalled for Packaging Violation
mGanna sodium hydroxide pellets sold on Amazon lack required child-resistant packaging, posing a risk of chemical burns and eye irritation. About 3,240 units were distributed from November 2024 through March 2026.
Product
mGanna Sodium Hydroxide (lye) Pellet Bags
Category
Consumer Product
Distribution
Distributed nationwide

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