FoodDec 31, 2025
Mellace Family Brands California 1) Wegmans Deluxe Mixed Nuts, Unsalted, Net Wt recall — FDA H-0337-2026
Potential contamination with Salmonella
Class IFDA: TerminatedMellace Family Brands California 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 3
Records are ordered by the best available source date.
FoodDec 31, 2025
Wegmans Food Markets Locatelli Pecorino Romano Cheese Grated recall — FDA H-0333-2026
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedWegmans Food Markets, Inc.
Medical DeviceDec 24, 2025
Rocket 18Fg Seldinger Catheter with Safety Guard recall — FDA Z-0953-2026
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Class IIFDA: OngoingRocket Medical Plc
Medical DeviceDec 24, 2025
GE Medical Systems China Co GE Healthcare Carestation anesthesia system Power Management recall — FDA Z-0915-2026
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC…
Class IFDA: OngoingGE Medical Systems China Co., Ltd.
Medical DeviceDec 24, 2025
AART Gluteal Implant Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style recall — FDA Z-0945-2026
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class IIFDA: OngoingDSAART LLC
Medical DeviceDec 24, 2025
AART Pectoral Implant Pectoral Implant recall — FDA Z-0948-2026
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class IIFDA: OngoingDSAART LLC
Medical DeviceDec 24, 2025
DICOM Grid Intelerad InteleShare software, with ProViewer component recall — FDA Z-0941-2026
Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in InteleShare viewer;…
Class IIFDA: OngoingDICOM Grid, Inc.
Medical DeviceDec 24, 2025
Medline Industries FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048 recall — FDA Z-0922-2026
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceDec 24, 2025
Copan Italia 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk recall — FDA Z-0943-2026
Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
Class IIFDA: OngoingCopan Italia
Medical DeviceDec 24, 2025
Medline Industries SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000 recall — FDA Z-0921-2026
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceDec 24, 2025
Medtronic MiniMed InPen App, Model/CFN Number: MMT-8061 (Android Users) recall — FDA Z-0958-2026
When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow notifications to override…
Class IIFDA: OngoingMedtronic MiniMed, Inc.
Medical DeviceDec 24, 2025
SEASPINE ORTHOPEDICS Orthofix NorthStar OCT Navigation Surgical Technique Guide, and recall — FDA Z-0937-2026
The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with the NorthStar OCT…
Class IIFDA: OngoingSEASPINE ORTHOPEDICS CORPORATION
Medical DeviceDec 24, 2025
Rocket 12Fg Seldinger Catheter Procedure Tray recall — FDA Z-0950-2026
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Class IIFDA: OngoingRocket Medical Plc
Medical DeviceDec 24, 2025
AART Chin Implant Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 recall — FDA Z-0946-2026
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class IIFDA: OngoingDSAART LLC
Medical DeviceDec 24, 2025
Xpert BCR-ABL Ultra recall — FDA Z-0959-2026
Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.
Class IIFDA: OngoingCepheid
Medical DeviceDec 24, 2025
GE Medical Systems China Co GE Healthcare Carestation anesthesia system, product number and recall — FDA Z-0914-2026
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC…
Class IFDA: OngoingGE Medical Systems China Co., Ltd.
Medical DeviceDec 24, 2025
AART Silicone Carving Implant Silicone Carving Implant Model/Catalog Numbers: 600-601 recall — FDA Z-0944-2026
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class IIFDA: OngoingDSAART LLC
Medical DeviceDec 24, 2025
Rocket 18Fg Seldinger Catheter Procedure Tray recall — FDA Z-0952-2026
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Class IIFDA: OngoingRocket Medical Plc
Medical DeviceDec 24, 2025
Copan Italia 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum recall — FDA Z-0942-2026
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
Class IIFDA: OngoingCopan Italia
Medical DeviceDec 24, 2025
Rocket 12Fg Seldinger Catheter with Safety Guard recall — FDA Z-0951-2026
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Class IIFDA: OngoingRocket Medical Plc
Medical DeviceDec 24, 2025
Fresenius Kabi USA Ivenix Infusion System (IIS), LVP Software LVP-SW-0005 recall — FDA Z-0885-2026
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.
Class IFDA: OngoingFresenius Kabi USA, LLC
Medical DeviceDec 24, 2025
Rocket 20Fg Seldinger Catheter Procedure Tray recall — FDA Z-0955-2026
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Class IIFDA: OngoingRocket Medical Plc
Medical DeviceDec 24, 2025
Datascope Cardiosave Hybrid recall — FDA Z-0931-2026
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
Class IIIFDA: OngoingDatascope Corp.
Medical DeviceDec 24, 2025
AART Malar Implant Malar Implant recall — FDA Z-0947-2026
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
Class IIFDA: OngoingDSAART LLC
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.