Recalls in 2024
By month
Most recalled brands
- Ford83
- Chrysler72
- Mercedes-Benz64
- BMW60
- Forest River59
- Dove52
By product type
- Vehicles2399
- Drugs & medical2016
- Cosmetics & chemicals1630
- Toys & kids1201
- Food & drink1003
- Electrical797
All recalls in 2024
- 2024-12-31
CA- CA
- CA
- CA
- 2024-12-30
USWinnebago Industries, Inc.: Entrance Door Window May Detach
A window that detaches during transit can become a road hazard, increasing the risk of a crash.
- CA
Newell Industries Canada Ltd. child car seat recall: other (Transport Canada 2024774)
Problem area: other. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.
Transport CanadaOfficial notice → - CA
Newell Industries Canada Ltd. child car seat recall: other (Transport Canada 2024773)
Problem area: other. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.
Transport CanadaOfficial notice → - CA
Canadian Motor Import Inc. restricted-use vehicle recall: powertrain (Transport Canada 2024772)
Problem area: powertrain. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.
Transport CanadaOfficial notice → - CA
Lamborghini car recall: engine (Transport Canada 2024771)
Problem area: engine. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.
Transport CanadaOfficial notice → - CA
Newell Industries Canada Ltd. child car seat recall: other (Transport Canada 2024768)
Problem area: other. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.
Transport CanadaOfficial notice → - CA
Fiat Chrysler Automobiles light truck & van recall: lights and instruments (Transport Canada 2024765)
Problem area: lights and instruments. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.
Transport CanadaOfficial notice → - CA
- CA
- CA
- CA
- CA
- CA
- CA
- 2024-12-27
UK- CA
- 2024-12-26
- US
GEM WAEV LLC: The Wheel May Separate From The Ball Joint
Ball joint separation can cause a loss of steering control, increasing the risk of a crash.
AUYuyu Pty Ltd - Bestore Pork Jerky Sesame Flavour 100g
The presence of an undeclared allergen (sesame).
FSANZOfficial notice →- US
BCI Burke Recalls Playground Merry-Go-Rounds Due to Crush Hazard
The space between the rotating platform and the stationary outer rim can leave a gap that narrows too much, posing a crushing hazard to children.
CPSCPlaydale Playgrounds LTD, of United KingdomAbout 415 (In addition, about 6 were sold in Canada)Official notice → - US
GIKPAL Dressers Recalled Due to Tip-Over and Entrapment Hazards; Violations of Federal Regulation for Clothing Storage Units; Sold Exclusively on Walmart.com by ONME…
The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate performance and warning…
- US
Precor Recalls Resolute™ Cable Multi-Station Exercise Equipment Due to Impact Injury Hazard
The pop-pin can fail to fully engage in the exercise equipment's vertical rail and cause the pulley carriage to drop unexpectedly during use, posing an impact injury hazard to users.
- US
Black Diamond Equipment Recalls PIEPS Pro IPS Avalanche Transceivers Due to Risk of Loss of Emergency Communications
The battery compartment within the avalanche transceiver could not have enough contact force to supply power. In some cases, the transceiver will fail to power on or cease operating during use. It would make it…
- 2024-12-25
- US
Mint Medical GmbH recalls mint Lesion, Software Versions: 3.9.0 through 3.9.5.
Some software versions have a malfunction where they may show incorrect orientation labels for a specific subset of DICOM images.
FDA · DeviceMint Medical GmbHWorldwide distribution: US (nationwide): AR, CA, FL, GA, MI, MN, NY, OH, PA,…Official notice → - US
Olympus Corporation of the Americas recalls Duravent Silicone Ventilation Tube. Model Number: 240075.
Potential that Duravent Silicone Ventilation Tubes may contain incorrect product, specifically, 1.32 mm Tiny T Tubes (model: 70240076) instead of the intended Duravent Silicone Ventilation Tubes.
FDA · DeviceOlympus Corporation of the AmericasAL, AZ, CA, IL, KY, MD, MN, MO, NC, ND, NY, OK, PA, SC, TN, TX, WA, WI.…Official notice → - US
GE OEC Medical Systems, Inc recalls OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging system used to…
Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
FDA · DeviceGE OEC Medical Systems, IncU.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA,…Official notice → - US
Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Multiport, Models: 1) Model # WC77, 2)…
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
- US
MicroPort Orthopedics Inc. recalls EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE…
Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls HUDSON RCI mBrace, ET Tube Holder with 4 Point Head Strap, REF DYNJMBRC4; tracheal tube fixation device
Complaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip which may cause dermal injury depending…
- US
Noah Medical recalls Galaxy System (GAL-001)
Bronchoscopic system uninterruptable power may have defective component, may cause power supply short circuit/trip protective circuit breakers causing sudden, unrecoverable power loss, which could occur while system is…
FDA · DeviceNoah MedicalUS: CA, MA, PA, NJ, ID, CT, MO, NC, MD, IL, TN, VA, OH, IN, WV, NYOfficial notice → - US
CooperSurgical, Inc. recalls Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An…
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
FDA · DeviceCooperSurgical, Inc.States: NC, NJ, TX, VA, IL, NY, CA, PA Please note: The countries below,…Official notice → - US
Philips North America Llc recalls Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216
The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to…
- US
Spacelabs Healthcare, Ltd. recalls Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the patient s ambulatory…
Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the…
FDA · DeviceSpacelabs Healthcare, Ltd.U.S.: AR, CA, CO, DE, FL, FA, LA, MA, MI, MN, MT, NC, NE, NU OH, OR, PA,…Official notice → - US
Spectranetics Corporation recalls Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm OTW 417-152 /…
Due to complaints received for the marker band detaching from the distal tip of the catheter and remaining in the patient as laser catheter was retracted.
FDA · DeviceSpectranetics CorporationU.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, ILIN, KS, KY,…Official notice → - US
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in…
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
FDA · DeviceDraeger Medical, Inc.No Atlan A300 or A300XL devices were imported into the US. Devices were direct…Official notice → - US
Medtronic Neurosurgery recalls Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM 27636 EXACTA W/BRAIDED CORD LOCK 27666…
Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS).
FDA · DeviceMedtronic NeurosurgeryWorldwide distribution. US nationwide including Puerto Rico; Algeria,…Official notice → - US
Kirwan Surgical Products, LLC recalls Optikon Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: OPT14-5011. Product Description: The Disposable Microsurgical…
Potential for the outer stainless-steel tube to break or detach.
FDA · DeviceKirwan Surgical Products, LLCWorldwide - US Nationwide including PUERTO RICO; AUSTRALIA, CANADA, CHILE,…Official notice →