FoodDec 31, 2025
Mondelez Global Ritz Peanut Butter Cracker Sandwiches, Net Wt recall — FDA H-0329-2026
Undeclared allergens (Peanut) due to mispackaging
Class IIFDA: TerminatedMondelez Global Llc
Latest records
Latest recalls — page 121
The newest recall records with useful source details are listed here.
FoodDec 31, 2025
A New Life Herbs 1:5 Alcohol Double Extract, Supports a healthy immune system recall — FDA H-0344-2026
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Class IIFDA: OngoingA New Life Herbs, LLC
FoodDec 31, 2025
A New Life Herbs Natural anti-inflammatory properties, supports gut, increases recall — FDA H-0346-2026
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Class IIFDA: OngoingA New Life Herbs, LLC
FoodDec 31, 2025
The James Skinner Publix Raspberry Coffee Cake, Net Wt recall — FDA H-0330-2026
Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label.
Class IIFDA: TerminatedThe James Skinner LLC
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
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
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026300 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories