FoodJan 8, 2025
Reser's Fine Foods FCF Item 404884, Gyro Kit With Trays recall — FDA F-0363-2025
Salmonella. Item 404884, Gyro Kit With Trays contains implicated cucumber in the tzatziki sauce 2oz. cup.
Class IFDA: TerminatedReser's Fine Foods, Inc.
January 2025 recalls — page 13
These records include useful source details for the selected month.
FoodJan 8, 2025
Heber Valley Artisan Cheese, LLC Cascade Raw Cheddar GTIN #90854115003059 packed in an recall — FDA F-0434-2025
The Cascade Raw Cheddar Cheese was recalled due to Shiga toxin-producing E. coli (STEC) and elevated generic E.coli in finished product testing results.
Class IFDA: TerminatedHeber Valley Artisan Cheese, LLC.
FoodJan 8, 2025
Gracie's Kitchens a.) King Kullen brand Tropical Fruit Cup recall — FDA F-0341-2025
Product may be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedGracie's Kitchens Inc.
FoodJan 8, 2025
RUSS DAVIS WHOLESALE Kowalski's Garden Salad Net Wt recall — FDA F-0371-2025
Cucumbers have potential to be contaminated with Salmonella.
Class IFDA: TerminatedRUSS DAVIS WHOLESALE
FoodJan 8, 2025
Grimmway Enterprises, Inc. dba Grimmway Farms --- Organic Baby Carrots --- Organic Baby recall — FDA F-0359-2025
Potential contamination with E. coli O121:H19
Class IFDA: TerminatedGrimmway Enterprises, Inc. dba Grimmway Farms
FoodJan 8, 2025
Reser's Fine Foods Beef & Lamb Gyro Sandwich Express Meal Kit recall — FDA F-0362-2025
Salmonella. Beef & Lamb Gyro Sandwich Express Meal Kit contains implicated cucumber in the tzatziki sauce 3oz. cup.
Class IFDA: TerminatedReser's Fine Foods, Inc.
DrugJan 8, 2025
Hikma Injectables USA phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL) recall — FDA D-0174-2025
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Class IIFDA: TerminatedHikma Injectables USA Inc
DrugJan 8, 2025
Hikma Injectables USA ketamine inj 50 mg per 1 mL recall — FDA D-0173-2025
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Class IIFDA: TerminatedHikma Injectables USA Inc
DrugJan 8, 2025
Levothyroxine Sodium Tablets, Lupin, 75 mcg (0.075mg), 1000 Tablets recall — FDA D-0167-2025
Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
VehicleJan 7, 2025
Tesla back over prevention software recall — NHTSA campaign 25V002000
Tesla, Inc. (Tesla) is recalling certain 2024-2025 Model 3, Model S, 2023-2025 Model X, and Model Y vehicles. The computer circuit board may short, resulting in the loss of the rearview…
back over prevention softwareTesla, Inc.
Medical DeviceJan 1, 2025
Nova Biomedical StatStrip Glucose Ketone Hospital Meter System recall — FDA Z-0682-2025
A software bug within the meter firmware leads to transmission of erroneous glucose and/or ketone patient test results to a healthcare institution's data management system (DMS) at…
Class IFDA: OngoingNova Biomedical Corporation
Medical DeviceJan 1, 2025
Becton, Dickinson and Company, BD Bio Sciences Device Description: FACSLyric 2L6C Instrument recall — FDA Z-0746-2025
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
Medical DeviceJan 1, 2025
Daytona Small Stature Ti Locking Cap 4.5mm, Small Stature, T25 recall — FDA Z-0752-2025
Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
Class IIFDA: OngoingSEASPINE ORTHOPEDICS CORPORATION
Medical DeviceJan 1, 2025
Siemens Healthcare Diagnostics epoc NXS Host; Siemens Material Number (SMN): 11413583 recall — FDA Z-0740-2025
Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System because of a software malfunction that occurs when specific criteria are met that can result in the incorrect…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJan 1, 2025
Siemens Healthcare Diagnostics epoc NXS Host; Siemens Material Number (SMN): 11413497 (EU) recall — FDA Z-0735-2025
Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System because of a software malfunction that occurs when specific criteria are met that can result in the incorrect…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJan 1, 2025
Becton, Dickinson and Company, BD Bio Sciences FACSLyric 3L8C Instrument US-IVD, Catalog recall — FDA Z-0747-2025
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
Medical DeviceJan 1, 2025
Straight Smile BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night recall — FDA Z-0750-2025
Virtual-only clinical workflow utilized for dental aligners and impression to approve patients for aligner devices may not be suitable for patients who have certain contraindications.
Class IIFDA: OngoingStraight Smile, LLC
Medical DeviceJan 1, 2025
Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS recall — FDA Z-0724-2025
Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJan 1, 2025
MEDLINE INDUSTRIES, LP - Northfield MAJOR NEURO PACK-LF Convenience kit, SKU DYNJ0578916X recall — FDA Z-0717-2025
Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJan 1, 2025
Becton, Dickinson and Company, BD Bio Sciences FACSLyric 3L10C Instrument US-IVD, Catalog recall — FDA Z-0748-2025
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
Medical DeviceJan 1, 2025
Siemens Healthcare Diagnostics epoc NXS Host; Siemens Material Number (SMN): 11413517(MX) recall — FDA Z-0738-2025
Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System because of a software malfunction that occurs when specific criteria are met that can result in the incorrect…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJan 1, 2025
Becton, Dickinson and Company, BD Bio Sciences FACSLyric 3L12C Instrument RUO, Catalog recall — FDA Z-0749-2025
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
Medical DeviceJan 1, 2025
O&M Halyard SOFT TOUCH II Surgical Mask, Blue-Disposable surgical mask Product Code: 47500 recall — FDA Z-0729-2025
Not meeting the bioburden testing requirements of EN 14683 required for masks sold in Europe. Face masks sold in the United States are not required to meet this standard. However, if the…
Class IIFDA: OngoingO&M HALYARD, Inc.
Medical DeviceJan 1, 2025
Becton, Dickinson and Company, BD Bio Sciences FACSLyric 2L4C Instrument US, Catalog Number recall — FDA Z-0745-2025
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.