The Recall Desk

Archive

July 2025 recalls

632 recalls were announced in July 2025.

What the numbers show

Critical
4
Severe
232
High
244
Moderate
144
Low
8

Of the 632 recalls this month scored against our rubric, 1% are Critical, 37% are Severe.

201–300 of 632

  • CriticalCPSC·25393·2025-07-21

    Above-ground pools recalled after nine children drowned using strap footholds

    Above-ground pools 48 inches and taller with compression straps over the vertical support legs are being recalled because the strap can create a foothold. CPSC believes nine children have drowned.

    Product
    48-inch and taller above-ground pools with compression straps running on the outside and over the vertical support legs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V475000·2025-07-21

    Rosenbauer Fire Trucks Recalled for Odometer Software Error

    Rosenbauer America is recalling 2019-2024 fire trucks because a software error may cause the odometer to freeze, potentially delaying critical safety maintenance.

    Product
    ROSENBAUER — ROSENBAUER WARRIOR, COMMANDER, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2025·2025-07-17

    Kayem Foods Recalls Chicken Sausage Due to Plastic Contamination

    Kayem Foods is recalling ready-to-eat chicken sausage products nationwide due to possible contamination with pieces of plastic.

    Product
    Kayem Foods Inc. — Kayem Foods Inc. Recalls Ready-To-Eat Chicken Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V473000·2025-07-17

    Grand Design trailer entrance door latch mechanism may fail

    Grand Design is recalling certain 2025-2026 Lineage trailers with Lippert Modularia entrance doors because the door latch mechanism may fail, potentially trapping occupants in an emergency.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25391·2025-07-17

    VIVI e-bike lithium-ion batteries can overheat, posing fire and burn hazards

    36-volt lithium-ion batteries supplied with certain VIVI e-bikes are being recalled because they can overheat. Fourteen overheating incidents including three fires have been reported. About 24,000 units affected.

    Product
    36-volt lithium-ion batteries used with VIVI E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25390·2025-07-17

    iStore magnetic wireless power banks can overheat and ignite while charging

    iStore Magnetic Wireless Power Banks, model IST-09991/W05, are being recalled because the lithium-ion battery can overheat and ignite while charging. Three incidents and about $15,000 in property damage reported.

    Product
    iStore Magnetic Wireless Power Banks (IST-09991/W05 model only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25389·2025-07-17

    CasaClean handheld steamers can leak steam or spew hot boiling water

    CasaClean Handheld Steamers, model DF-958, are being recalled because they can leak steam or spew hot boiling water. Thirteen consumers have received burns. About 23,000 units are affected.

    Product
    CasaClean Handheld Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25387·2025-07-17

    Traveller aluminum loading ramps can bend or break under rated loads

    Traveller aluminum loading ramps are being recalled because they cannot withstand the weight specified on the ramps and can bend or break in use. Two injuries have been reported. About 18,000 units affected.

    Product
    Traveller Aluminum Loading Ramps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V472000·2025-07-17

    Jeep Grand Cherokee second-row head restraints may not lock upright

    Chrysler is recalling certain 2023-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because the second-row head restraints may not lock in the upright position, failing FMVSS 202.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25388·2025-07-17

    Primark Stitch scented highlighters contain phthalates above the federal ban

    Primark DTR Stitch Scented Highlighters 4-packs are being recalled because they contain phthalates in violation of the federal phthalates ban. About 2,600 units are affected.

    Product
    Primark DTR (direct-to-retail) Stitch Scented Highlighters (4-pack)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25392·2025-07-17

    Babyletto Kiwi recliner USB modules can overheat and spark in use

    Babyletto Kiwi Electronic Recliner and Swivel Gliders are being recalled because the USB module in the recliner arm can overheat and spark. About 9,030 units are affected.

    Product
    Babyletto Kiwi Electronic Recliner and Swivel Gliders with USB port
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V471000·2025-07-17

    Chrysler Pacifica built with wrong radio may not show rearview image

    Chrysler is recalling certain 2024-2025 Pacifica vehicles that were built with an incorrect radio, which can prevent the rearview camera image displaying. All affected vehicles have been repaired.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V474000·2025-07-17

    Genesis G90 and GV60 instrument panel display can fail

    Hyundai is recalling certain 2023-2025 Genesis G90 and GV60 vehicles because a software error may cause the instrument panel display to fail, failing FMVSS 101.

    Product
    GENESIS — GENESIS GV60, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E044000·2025-07-17

    Chrysler Recalls Mopar Second-Row Head Restraints for Locking Defect

    Chrysler is recalling Mopar second-row head restraints that may not lock in the upright position, increasing injury risk during a crash.

    Product
    SEATS:MID/REAR ASSEMBLY:HEAD RESTRAINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0216-2025·2025-07-16

    Weaver white seed nonpareil chocolate recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate (White Seeds) in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 1,760 cases are affected.

    Product
    Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate (White Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·H-0213-2025·2025-07-16

    JLM dark chocolate nonpareils recalled over undeclared milk allergen

    JLM Manufacturing Dark Chocolate Nonpareils in 14 oz tubs are being recalled because of undeclared milk. 971 cases are affected, distributed nationwide.

    Product
    JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2085-2025·2025-07-16

    FEM-FLEX II FEMII018AS cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018AS, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 558 units affected.

    Product
    Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS Software Version: N/A Product Description: The Edwards FEMFLEXII Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2080-2025·2025-07-16

    Optisite OPTI16 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI16 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 27,022 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2083-2025·2025-07-16

    FEM-FLEX II femoral arterial cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2032-2025·2025-07-16

    Hillrom LikoScale patient lift components may falsely latch and detach

    Hillrom LikoScale components used with patient lift adapter kits are being recalled because the Q-link 13 may allow false latching of the quick-release hook. 9,839 units are affected.

    Product
    Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·25V470000·2025-07-16

    BMW electric vehicle battery modules may be improperly assembled

    BMW is recalling certain 2022-2025 iX, 2023-2024 i7 and 2022-2023 i4 vehicles because high-voltage battery cell modules may not have been assembled properly, stressing the module frame.

    Product
    BMW — BMW I4, I7, IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0214-2025·2025-07-16

    Garlic cheddar cheese curds recalled over potential Listeria monocytogenes contamination

    Vampire Slayer Garlic Cheddar Cheese Curds are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 260 cases are affected.

    Product
    VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup with lid. UPC on 6oz. retail cup: 8 51222 00528 7. FaceRockCreamery.com MASTER CASE's label is read in parts: Item No. 240062 Vampire Slayer Curds 12/6oz., net wt. 4.5 lbs. Face
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0221-2025·2025-07-16

    Whole organic celery seed recalled over potential Salmonella contamination

    Whole Organic Celery Seed is being recalled because of potential contamination with Salmonella. 439 bags totalling 24,694 lbs are affected.

    Product
    Celery Seed Whole Organic, labeled, "CELERY SEED WHL OG; Net Wt: 56.25 Lbs"
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0215-2025·2025-07-16

    Weaver bulk semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.

    Product
    Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2031-2025·2025-07-16

    Hillrom Q-Link 13 patient lift components may falsely latch and detach

    The Hillrom Q-Link 13 component used with mobile patient lifts is being recalled because it may allow false latching of the quick-release hook. 9,899 units are affected.

    Product
    Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile lift - Product Code 2010004; 2) Viking L Mobile lift - Product Code 2040044; 3) Viking XL Mobile lift - Product Code 2040043; 4) Viking M Mobile lift -
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2082-2025·2025-07-16

    FEM-FLEX II FEMII016A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII016A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 6,801 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2047-2025·2025-07-16

    Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction

    The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.

    Product
    Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2084-2025·2025-07-16

    FEM-FLEX II FEMII018A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2025·2025-07-16

    VersaCross RF wire lots may have a punctured sterile barrier pouch

    The VersaCross RF Wire is being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units are affected.

    Product
    VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device approved and commercialized in Japan only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2108-2025·2025-07-16

    Alcon Constellation vitrectomy packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2097-2025·2025-07-16

    Infinia nuclear medicine systems may show unintended radial detector motion

    Infinia, Infinia Hawkeye, Infinia II and Infinia II Hawkeye 4 nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software. 1,822 units affected.

    Product
    Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye 4 Nuclear Medicine system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0258-2025·2025-07-16

    Ghouribeh date rolls recalled over undeclared wheat, soy and sesame

    C Sweet Ghouribeh Rolls with date, sesame and pistachios are being recalled because wheat, soy and sesame are undeclared. 30 units are affected.

    Product
    C Sweet Ghouribeh Rolls with date, sesame, & pistachios 10 oz., UPC 642896991132
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2106-2025·2025-07-16

    Torflex transseptal guiding sheath kits may have a punctured sterile pouch

    Torflex Transseptal Guiding Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0218-2025·2025-07-16

    Wegmans blueberry mini muffins may contain foreign objects of metal origin

    Wegmans brand Blueberry Mini Muffins family pack is being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789053227
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2105-2025·2025-07-16

    VersaCross transseptal sheath kits may have a punctured sterile barrier pouch

    VersaCross Transseptal Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS 63CM/45DEG/D0 SHEATH VXS2112 VERSACROSS SHEATH (63CM 45DEG D0)-J Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, includ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0278-2025·2025-07-16

    Wegmans semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Wegmans Semi-Sweet Chocolate Nonpareils are being recalled because of undeclared milk. 595 cases are affected across nine states and the District of Columbia.

    Product
    Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ (1 LB 2.5 OZ) (524 g), packaged in a plastic tub and packed 12 per case, Distributed by: Wegmans Food Markets, Inc. Rochester, NY 14603. Ingredients: Sugar, Chocolate Liquor, Cacao Fat, Corn Starch, Soy Lecithin (emulsifier
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2110-2025·2025-07-16

    Alcon Custom Pak surgical kits may have damaged lidding compromising sterility

    Alcon Custom Paks, customer-designed sterile surgical kits, are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 15,557 kits affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience kits intende
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2109-2025·2025-07-16

    Alcon Constellation procedure packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Combined Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 89,495 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Combined Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0320-2025·2025-07-16

    Crown Point shelled edamame recalled because the label does not declare soy

    Crown Point Shelled Edamame in 22 lb cases is being recalled because the label declares shelled edamame but does not specify or declare soy. 1,046 cases are affected.

    Product
    Crown Point Shelled Edamame, net wt. 22lbs. UPC 813973 01840 4. Product is packaged in carton box with poly liner. Distributed by Alpine Foods Distributing Inc. Milwaukie, OR. Product of China.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·H-0219-2025·2025-07-16

    Wegmans French toast mini muffins may contain foreign objects of metal

    Wegmans brand French Toast Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    a. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 22 OZ (1 LB 6 OZ) 624 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789058612 b. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 13 OZ (369 g); packaged in plastic clamshell; UPC: 7789052435
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0220-2025·2025-07-16

    Wegmans chocolate chip mini muffins may contain foreign objects of metal

    Wegmans brand Chocolate Chip Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; CHOCOLATE CHIP; NET WT 13.5 OZ; packaged in plastic clamshell; UPC 7789053223
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2101-2025·2025-07-16

    O-arm O2 imaging system gantry support may have been damaged

    The O-arm O2 Imaging System is being recalled because a mechanical component supporting the gantry to the support structure may have been damaged during manufacture. 3 units affected.

    Product
    O-arm O2 Imaging System. Mobile X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2025·2025-07-16

    Nuclear medicine systems may show unintended radial detector motion during scans

    Varicam, Millennium VG, Millennium VG Hawkeye and Discovery VH nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software version. 21 units affected.

    Product
    Varicam, Millennium VG, Millennium VG Hawkeye, Discovery VH Nuclear Medicine System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2025·2025-07-16

    VersaCross access kits may have a hole in the sterile pouch

    VersaCross Access Solution kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF WIRE 63CM/45DEG/D1) VXSK0102 VXSK (180J RF WIRE 63CM/55DEG/D0) VXSK0103 VXSK (180P RF WIRE 63CM/45DEG/D0) VXSK0121 VXSK (180P RF WIRE 63CM/45DEG/D1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2099-2025·2025-07-16

    Canturio smart tibial stem extensions recalled over an incorrect product label

    Canturio Smart Extension CSE Implants are being recalled due to a labeling error, with the product incorrectly labeled. 106 units are affected.

    Product
    Brand Name: Canturio¿ Smart Extension Product Name: CSE Implant Model/Catalog Number: 43-5570-030-14 Product Description: Tibial stem extension for use with Zimmer Persona¿ Personalized Knee System; 14mm diameter x 30mm height. Implantable device with integrated electronics fo
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0514-2025·2025-07-16

    GreenScreen zinc oxide sunscreen recalled over manufacturing practice deviations

    GreenScreen organic zinc oxide sunscreen SPF 32 is being recalled because of cGMP deviations. 174 tubes are affected.

    Product
    GreenScreen, kabana organic skincare, Bread Spectrum UVA & UVB, Zinc Oxide Sunscreen, Organic Ingredients, Fragrance Free, Biodegradable, Chemical Free, Non-Nano, Baby Safe, Original, SPF 32, Totally Green personal care, Zinc Oxide USP 25%, 3.4 FL OZ/115 G Tube, NDC: 73369-0001-1
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2092-2025·2025-07-16

    TrueDent dental resin cartridges carry a formatting error in expiration dates

    TrueDent Magenta dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 94 units are affected.

    Product
    TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0224-2025·2025-07-16

    Bicolor sweet corn recalled over possible reach truck fluid contamination

    Florida bicolor sweet corn and eastern bi-color tray pack corn are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. FLORIDA BICOLOR SWT CORN 2. EASTERN BI-COLOR TRAY PACK
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0512-2025·2025-07-16

    B Natural Organics mineral sunscreens recalled over manufacturing practice deviations

    B Natural Organics Organic Sunscreen SPF 30, in tinted and tint free formulas, is being recalled because of cGMP deviations. 204 tubes are affected.

    Product
    B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1002-2; b) Tint Free Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1001-2; c)
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Food)·H-0232-2025·2025-07-16

    Organic broccoli bunches and crowns recalled over reach truck fluid contamination

    Organic broccoli bunches, wrapped broccoli and broccoli crowns are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. BROCCOLI OG2 BROCCOLI BUNCH 2. WLD HRVST OG2 BROCCOLI WRPP 3. USA OG2 BROCCLI CRWNS
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0253-2025·2025-07-16

    Daniele extra virgin olive oil is likely canola oil instead

    Daniele brand First Cold Press Extra Virgin Olive Oil in 3 L containers is being recalled because the product is likely canola oil, not extra virgin olive oil. 10 cases are affected.

    Product
    Daniele brand First Cold Press EXTRA VIRGIN OLIVE OIL; NET 101.4 FL. OZ. (3 QT. 5.4 FL. OZ.) 3L; IMPORTED; Distributed by: dfs international ltd Springfield, ma 01104; INGREDIENTS: EXTRA VIRGIN OLIVE OIL; Product contains select high quality Extra Virgin Olive Oil from the countr
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0222-2025·2025-07-16

    Red Delicious, Gala and organic apples recalled over reach truck fluid

    A range of apples, including Red Delicious, Gala, Granny Smith and Fuji, is being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. USA APLS RED DEL TOTE 2. USA APLE RED DEL 80CT 3. DOMESTIC APPLE GALA TOTES 4. USA APPLES GALA 80CT 5. WLD HRVST OG2 WAXF GRNY SMTH 6. WLD HRVST OG2 WAXF FUJI 7. WLD HRVST OG2 WAXF GALA 8. WLD HRVST OG2 WAXF PINK LADY 9. WA OG1 HNYC
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2090-2025·2025-07-16

    TrueDent Clear dental resin cartridges carry an expiration date formatting error

    TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.

    Product
    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2025·2025-07-16

    In Your Face tinted mineral sunscreen recalled over manufacturing practice deviations

    In Your Face Mineral Tint SPF 31 tinted sunscreen is being recalled because of cGMP deviations. 76 bottles are affected.

    Product
    In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingredients, Biodegradable & Baby Safe, 50 mL - 1.7 fl oz per bottle, Manufactured for IN YOUR FACE Skin Care, Belleair Bluffs, FL, Made in USA, NDC: 73369-1601-1
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Food)·H-0234-2025·2025-07-16

    Organic red and green cabbage recalled over reach truck fluid contamination

    Organic red and green cabbage is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. WLD HRVST OG2 RED CABBAGE 2. USA/MX OG2 RED CABBAGE 3. USA ORGC GRN CABBAGE 4. WLD HRVST OG2 GREEN CABBAGE
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0229-2025·2025-07-16

    Kale bunches recalled over possible contamination with reach truck fluid

    Kale bunches, including organic and lacinato kale, are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. USA KALE BUNCH CTN 2. USA OG2 KALE 3. USA OG1 LACINATO KALE
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0223-2025·2025-07-16

    Organic and conventional carrots recalled over possible reach truck fluid contamination

    A range of carrot products is being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. BLTHSFRSH CARROT CRINKLE 2. OG2 RNBW BNCH CRTS 3. OG2 GRN TOP CARRO 4. ORGC JUMBO CARRO 5. OG2 CARROTS BAG 6. OG2 CARROTS BAG 7. OG2 CARROTS BAG 8. WLD HRVST OG2 CELLO CARROTS 9. OG1 PETITE CARROT 10. USA OG1 BBY PLD CARRT 11. WLD HRVST OG2 BBY
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2100-2025·2025-07-16

    Hummingbird stimulated EMG kit packaging shows the wrong part number

    The Hummingbird Stimulated EMG Kit is being recalled because the product packaging contains the wrong part number and kit contents. 10 units are affected.

    Product
    Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Single-Use Bipolar Minifork Stimulation Probe, 90mm, and 1 Green Ground Needle ; REF 1-D-BMF90-5, lot number 050925219, expiration 2028-11-30 I-D-BMF90-5 Stim
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2091-2025·2025-07-16

    TrueDent Cyan dental resin cartridges carry an expiration date formatting error

    TrueDent Cyan dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 100 units are affected.

    Product
    TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0509-2025·2025-07-16

    Famciclovir tablets recalled after a hair was found on a tablet

    Famciclovir Tablets USP 500 mg from Macleods Pharma are being recalled because a black hair strand was found attached to a tablet in a sealed bottle. 9,888 bottles are affected.

    Product
    FAMCICLOVIR — FAMCICLOVIR (FAMCICLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0513-2025·2025-07-16

    Erin's Faces mineral sunscreen recalled over manufacturing practice deviations

    Erin's Faces Mineral SPF 32 sunscreen is being recalled because of cGMP deviations. 54 tubes are affected.

    Product
    Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide, 3 FL OZ/ 85 mL per bottle, Made in USA for Erin's Faces, Millburn, NO 07041. NDC: 73369-1401-1
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Food)·H-0235-2025·2025-07-16

    Organic bok choy recalled over possible reach truck fluid contamination

    Organic bok choy and organic baby bok choy are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. USA ORGC BOK CHOY 2. USA/MEX OG2 BABY BOKCHOY
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2093-2025·2025-07-16

    TrueDent Yellow dental resin cartridges carry an expiration date formatting error

    TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.

    Product
    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2094-2025·2025-07-16

    TrueDent White dental resin cartridges carry an expiration date formatting error

    TrueDent White dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 109 units are affected.

    Product
    TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0242-2025·2025-07-16

    Organic leaf lettuce and romaine recalled over reach truck fluid contamination

    Organic red leaf lettuce, green romaine, butter lettuce and living butter lettuce are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. CA OG2 RED LF W/TAG 2. CA OG2 GR ROMN W/TG 3. USA/MEX OG2 BUTTER LETTCE 4. USA OG2 LIVING BUTTER
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0259-2025·2025-07-16

    Shoppers Value fruit cocktail recalled over undeclared Red No. 3 colour

    Shoppers Value Fruit Cocktail in heavy syrup is being recalled because of undeclared Red No. 3 (E127). 1,105 cases are affected.

    Product
    SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per case.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·H-0228-2025·2025-07-16

    Curly and Italian parsley recalled over possible reach truck fluid contamination

    Curly parsley and Italian parsley, including organic Italian parsley, are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. CA CURLY PARLSEY CTN 2. CA ITALIAN PARSLEY 3. USA OG2 ITALN PARSLEY
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0252-2025·2025-07-16

    Calais grape jelly contains undeclared FD&C Blue 1 and Red 40

    Calais brand Grape Jelly in 1 gallon containers is being recalled because it contains undeclared colours FD&C Blue 1 and FD&C Red 40. 43 cases are affected.

    Product
    Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGREDIENTS: Grape Juice, Corn Syrup, High Fructose Corn Syrup, Pectin, Citric Acid; REFRIGERATE AFTER OPENING; UPC 040264 10128 0
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0237-2025·2025-07-16

    Organic celery products recalled over possible reach truck fluid contamination

    Organic celery products, including sleeved celery, naked celery and celery hearts, are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. WLD HRVST OG2 SLVD CELERY 2. USA OG2 NAKED CELERY 3. WLD HRVST OG2 CELERY HRT US
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2107-2025·2025-07-16

    Preat Astra dental analogs have rotational feature 180 degrees off

    Preat Astra EV-compatible 4.2 mm Digital Analogs are being recalled because a manufacturing error left the digital analog rotational feature 180 degrees off. 44 units are affected.

    Product
    Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V415000·2025-07-15

    Porsche suspension strut retaining ring can loosen dislodging the strut

    Porsche is recalling certain 2025 Panamera, Panamera E-Hybrid and Taycan vehicles because a retaining ring on top of the suspension strut may come loose, dislodging the strut and losing air from the spring.

    Product
    PORSCHE — PORSCHE TAYCAN, PANAMERA, PANAMERA 4 E-HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide

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