FoodOct 2, 2024
Skagit River Bakery & Cafe Marionberry Scones, bulk packaged in cake boxes with parchment recall — FDA F-1831-2024
Undeclared soy lecithin and soybean oil on label
Class IIFDA: TerminatedSkagit River Bakery & Cafe
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 46
Records are ordered by the best available source date.
FoodOct 2, 2024
Niitakaya USA Miso Katsuo Ninniku recall — FDA F-1834-2024
Undeclared allergen (Fish) Ingredient
Class IIFDA: TerminatedNiitakaya USA Inc.
FoodOct 2, 2024
M & P Food Productions M&P Delicacies PIROZHKI recall — FDA F-1825-2024
Products contain undeclared sub ingredients: wheat and milk
Class IIFDA: TerminatedM & P Food Productions, Ltd.
VehicleOct 2, 2024
BMW electronic stability control (esc) recall — NHTSA campaign 24V739000
BMW of North America, LLC. (BMW) is recalling certain 2023-2024 X1, X5, X6, X7, XM, 530i, i5, 740i, 760i, i7, and 750e vehicles. Please see the recall report for a complete list of models…
electronic stability control (esc)BMW of North America, LLC
DrugOct 2, 2024
AbbVie Refresh LACRI-LUBE recall — FDA D-0665-2024
Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.
Class IIFDA: OngoingAbbVie Inc.
DrugOct 2, 2024
SHEET SPF 30 MINERAL Vivier Sheer SPF 30 Mineral With Antioxidants recall — FDA D-0662-2024
Microbial Contamination of Non-Sterile Product
Class IIFDA: OngoingVivier Pharma, Inc.
DrugOct 2, 2024
Guru Infla-650 Herbal Dietary Supplement, 700mg recall — FDA D-0666-2024
Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
Class IIFDA: OngoingGuru Inc.
DrugOct 2, 2024
AbbVie Refresh P.M recall — FDA D-0664-2024
Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.
Class IIFDA: OngoingAbbVie Inc.
VehicleOct 1, 2024
Ram 1500 steering control module recall — NHTSA campaign 24V729000
Chrysler (FCA US, LLC) is recalling certain 2023-2024 Ram 1500 vehicles. The turn signal self-canceling feature may not function properly. As such, these vehicles fail to comply with the…
steering control moduleChrysler (FCA US, LLC)
Medical DeviceSep 25, 2024
GE Healthcare GmbH ViewPoint; system, imaging processing, radiological recall — FDA Z-3145-2024
The National Institute of Standards and Technology (NIST) has identified in the National Vulnerability Database (NVD) that NexGen Healthcare Mirth Connect, prior to version 4.4.1, has a…
Class IIFDA: OngoingGE Healthcare GmbH
Medical DeviceSep 25, 2024
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) recall — FDA Z-3160-2024
Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as…
Class IIFDA: OngoingGE Healthcare
Medical DeviceSep 25, 2024
Boston Scientific Flexima APDL Drainage Catheter System and Kit, Material Numbers: a) REF recall — FDA Z-3147-2024
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceSep 25, 2024
B Braun Medical STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to transfer blood recall — FDA Z-3179-2024
Incomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback…
Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceSep 25, 2024
Cypress Medical Products General Purpose Syringe McKesson 60 mL Luer Lock Tip Without recall — FDA Z-3154-2024
The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were…
Class IIFDA: OngoingCypress Medical Products LLC
Medical DeviceSep 25, 2024
B. Braun Medical AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual recall — FDA Z-3144-2024
Potential for product leakage from the Spin Lock Connector on the distal end of the device due to the migration of excess solvent during the assembly process.
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceSep 25, 2024
Smith & Nephew DIAMOND POINT, BOTH ENDS K-WIRE, REF 128062, metallic bone fixation fastener recall — FDA Z-3172-2024
Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contained K-WIRE…
Class IIFDA: OngoingSmith & Nephew, Inc.
Medical DeviceSep 25, 2024
UNIMAX MEDICAL SYSTEMS 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF recall — FDA Z-3164-2024
The tube may fall into the surgical site during the grasping process.
Class IIFDA: OngoingUNIMAX MEDICAL SYSTEMS Inc.
Medical DeviceSep 25, 2024
MICROVENTION ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device recall — FDA Z-3157-2024
Due to Retrieval Device product labels stating the incorrect expiration dates that (5 years instead of 3 years) which extends beyond their true expiration date.
Class IIFDA: OngoingMICROVENTION Inc.
Medical DeviceSep 25, 2024
Baxter EXACTAMIX Inlet, Non-Vented, High Volume Inlet, REF H938173, for use in a recall — FDA Z-3082-2024
Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174,…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceSep 25, 2024
CareFusion 303 Alaris Syringe Module Model 8110, a modular infusion pump and monitoring recall — FDA Z-3141-2024
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceSep 25, 2024
B Braun Medical STREAMLINE BLOODLINE LONG VERSION, FMC-Tubing to be used to transfer blood recall — FDA Z-3176-2024
Incomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback…
Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceSep 25, 2024
Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument recall — FDA Z-3156-2024
Software anomalies which can result in two separate issues: A lagging screen display during a navigated procedure; or the potential for a mismatch between the navigated screw and the screw…
Class IIFDA: OngoingMazor Robotics Ltd
Medical DeviceSep 25, 2024
Btt Health Gmbh Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser recall — FDA Z-3162-2024
Some power supply units in Austria and Germany had a voltage drop in the millisecond range, which led to a cancellation of the treatment and subsequent restart of the medical device. The…
Class IIFDA: OngoingBtt Health Gmbh
Medical DeviceSep 25, 2024
Smith & Nephew DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener recall — FDA Z-3171-2024
Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contained K-WIRE…
Class IIFDA: OngoingSmith & Nephew, Inc.
About the 2024 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.