DrugJul 23, 2025
Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 90-count bottle recall — FDA D-0518-2025
Subpotent Drug: Assay below the approved specification
Class IIFDA: OngoingACCORD HEALTHCARE, INC.
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 76
Records are ordered by the best available source date.
DrugJul 23, 2025
Rizatriptan Benzoate Tablets, USP, 10 mg, 18 (3x6) Unit Dose Tablets recall — FDA D-0534-2025
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Class IIFDA: OngoingAscend Laboratories, LLC
DrugJul 23, 2025
Central Admixture Pharmacy Services, Inc (CAPS) PERIPHERAL PARENTERAL NUTRITION, Compounded recall — FDA D-0530-2025
Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.
Class IIFDA: OngoingCentral Admixture Pharmacy Services, Inc (CAPS) Los…
DrugJul 23, 2025
Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottle recall — FDA D-0523-2025
Subpotent Drug: Assay below the approved specification
Class IIFDA: OngoingACCORD HEALTHCARE, INC.
DrugJul 23, 2025
Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles recall — FDA D-0532-2025
Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet…
Class IIFDA: OngoingLupin Pharmaceuticals Inc.
VehicleJul 17, 2025
Chrysler head restraint recall — NHTSA campaign 25V472000
Chrysler (FCA US, LLC) is recalling certain 2023-2024 Jeep Grand Cherokee and Jeep Grand Cherokee L vehicles. The second-row seat head restraints may not lock in the upright position. As…
head restraintChrysler (FCA US, LLC)
Medical DeviceJul 16, 2025
Optisite Arterial Cannula recall — FDA Z-2081-2025
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Class IFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceJul 16, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Varicam, Millennium VG, Millennium VG Hawkeye recall — FDA Z-2098-2025
Unintended radial detector motion may occur during patient setup or during patient scan if system does not have correct version of gantry software installed. Unintended detector motion may…
Class IIFDA: OngoingGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Medical DeviceJul 16, 2025
STRATASYS TrueDent White, TDM110, Model No recall — FDA Z-2094-2025
Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and…
Class IIIFDA: CompletedSTRATASYS LTD
Medical DeviceJul 16, 2025
STRATASYS TrueDent Magenta, TDM130, Model No recall — FDA Z-2092-2025
Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and…
Class IIIFDA: CompletedSTRATASYS LTD
Medical DeviceJul 16, 2025
Alcon Laboratories, Inc. Custom Pak recall — FDA Z-2110-2025
Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the…
Class IIFDA: OngoingAlcon Research LLC
Medical DeviceJul 16, 2025
Hummingbird Stimulated EMG Kit with Hummingbird recall — FDA Z-2100-2025
Product packaging contains the wrong part number and kit contents.
Class IIFDA: OngoingNeurovision Medical Products Inc.
Medical DeviceJul 16, 2025
FEM-FLEXII Femoral Arterial Cannula recall — FDA Z-2085-2025
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Class IFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceJul 16, 2025
FEM-FLEX II Femoral Arterial Cannula recall — FDA Z-2082-2025
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Class IFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceJul 16, 2025
Alcon Laboratories, Inc. Constellation Vision System Combined Procedure Pak recall — FDA Z-2109-2025
Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the…
Class IIFDA: OngoingAlcon Research LLC
Medical DeviceJul 16, 2025
Preat recall — FDA Z-2107-2025
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
Class IIFDA: OngoingPreat Corp
Medical DeviceJul 16, 2025
Baxter Healthcare Hillrom Q-Link 13 component, Product Code 3156509, used with the following recall — FDA Z-2031-2025
The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 16, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Infinia, Infinia Hawkeye, Infinia II, Infinia recall — FDA Z-2097-2025
Unintended radial detector motion may occur during patient setup or during patient scan if system does not have correct version of gantry software installed. Unintended detector motion may…
Class IIFDA: OngoingGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Medical DeviceJul 16, 2025
STRATASYS TrueDent Cyan, TDM 120, Model No recall — FDA Z-2091-2025
Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and…
Class IIIFDA: CompletedSTRATASYS LTD
Medical DeviceJul 16, 2025
Baxter Healthcare Hillrom LikoScale component, Product Code 3156232, used with the following recall — FDA Z-2032-2025
The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 16, 2025
STRATASYS TrueDent Yellow, TDM140, Model No recall — FDA Z-2093-2025
Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and…
Class IIIFDA: CompletedSTRATASYS LTD
Medical DeviceJul 16, 2025
Alcon Laboratories, Inc. Constellation Vision System Vitrectomy Procedure Pak recall — FDA Z-2108-2025
Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the…
Class IIFDA: OngoingAlcon Research LLC
Medical DeviceJul 16, 2025
Given Imaging Bravo CF capsule delivery device, designed to place and attach a pH monitoring recall — FDA Z-2047-2025
It has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule from…
Class IFDA: OngoingGiven Imaging Ltd.
Medical DeviceJul 16, 2025
Boston Scientific VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 recall — FDA Z-2105-2025
Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case…
Class IIFDA: OngoingBoston Scientific Corporation
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.