2024 Product Recalls
4,022 recalls issued in 2024.
Showing 3821–3840 of 4,022 recalls
Herold's Salad - Original Potato Salad packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
Potential contamination with Listeria monocytogenes
Organic Low/Reduced Sodium Chicken Broth sold under: O Organics 32oz Organic Low Sodium Chicken Broth Central Market, 32oz Organic Low Sodium Chicken Broth Lidl, 32oz Organic Low Sodium Chicken Broth
potential microbial contamination
Cheddar Kettle Corn, Net Wt 10 Oz (283 g), Ingredients: Locally-Farmed Corn, Corn Oil, Sugar, Salt, 100% Cheddar Powder
Cheddar Popcorn label does not declare milk or sub-ingredients, Maltodextrin, Sunflower oil, Yellow #5, Yellow #6, and Lactic Acid.
Herold's Salad - Original Potato Salad with egg packaged in 8oz, 1lb, 2lb, 5lb, and 10lb plastic containers
Potential contamination with Listeria monocytogenes
Trader Joe's 32oz Turkey Stock
potential microbial contamination
Wellsley Farms Assorted Mini Quiches NET WT 36 OZ (2LB 4 OZ) 1.02kb Keep Frozen UPC: 8867002630. Packaged in plastic trays in a cardboard box. 2 sealed trays in a box, 10 boxes per case
Possible foreign material (aluminum)
Natures Promise, 32oz Organic Vegetable Stock
potential microbial contamination
Herold's Salads - Greek Gemelli Pasta Salad packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
Potential contamination with Listeria monocytogenes
Organic Chicken Broth sold under: 365 Organic, 32oz Chicken Broth, Good & Gather, 32oz Organic Chicken Broth Sprouts, 32oz Organic Chicken Broth Natures Promise, 32oz Organic Chicken Stock Market Basket, 32oz Organic Chicken Stock O Organics, 32oz Organic Chicken Broth
potential microbial contamination
Rearview Image May Not Display
A rearview image that does not display while in reverse decreases the driver's visibility and increases the risk of a crash.
Tesla has released an over-the-air (OTA) software update, free of charge. Owner notification letters were mailed March 22, 2024. Owners may contact Tesla customer service at 1-877-798-3752. Tesla's number for this recall is SB-24-00-002.
Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid chromatography-tandem mass spectrometry (LC-MS/MS) systems. Model No. 5088288
The values of the Internal Standard (IS) concentrations are incorrectly derived when the user builds a customized test, then set the IS column to hidden and left the column empty. This may lead to the user making incorrect conclusions using incorrect results.
On October 4, 2021, the firm distributed Urgent Medical Device Correction letters to affected consignees. Customers were provided with temporary actions that could be implemented for safe handling of the recalled software to prevent the reporting of incorrect results to healthcare providers resulting in incorrect conclusions: 1. Avoid setting the IS (Internal Standard) column as hidden AND leaving it empty 2. Review values in the IS Concentration column 3. Follow lab SOPs to ensure quality control SCIEX is working on the hotfix for Cliquid MD Software version 3.4 and will contact affected customers as soon as it is ready The hotfixes may be downloaded free of charge directly from SCIEX s website, at the following location: https://sciex.com/software-support/software-downloads Software release notes will provide detailed installation instructions for installing the Hotfix. If you have any questions, please contact customer service at 1-877-740-2129, option 1, and then option 4, or your local SCIEX support number. You may also submit questions through their web portal at https://sciex.com/request-support.
Vial2BagDC, Product Number 6070112. The 20mm Vial2Bag DC device, is intended for use in healthcare facilities or in-home environment by the patient or care-giver to aid and support prescribed treatment and therapy. The device consists of the Vial2Bag piercing spike and cover, the IV Port connector and an integrated Vial Adapter (20mm) for access to the drug/solution vial.
Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process.
The recalling firm's sent an Urgent Medical Device Recall Letter dated October 13, 2017. was supplied to the consignee which contains the instructions for the recall process to the consignee. The notification letter will be sent to the Distributor via email. The notification letter instructs the distributor to notify the Customer/Users via the Medimop consignee recall letter. For further questions, please call (610) 594-4353.
ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model number
FDA review concluded that the test is insufficiently supported by clinical performance data, and results reported may not have been accurate (false positives or false negatives).
On April 17, 2022, the firm notified affected physicians who had ordered tests and received results since September 2020 via email. Customers were informed that the prior test results may not have been accurate. In addition, customers were instructed to check their stock and destroy any remaining Dried Blood Spot Collection Kits (ProterixBio SARS-CoV-2 RBD Antibody Test sampling kits). Customers should note the number of kits destroyed in their response to the recalling firm. For questions and clarifications regarding this notification please call ProterixBio at 978-901-6649 or email support@proterixbio.com. Business hours are 8 am to 4:30 pm, Eastern Time.
Centrella Smart+ Bed, Catalog Number P7900
The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse call wall unit.
On April 30, 2020, the firm distributed Urgent Medial Device Correction letters to affected customers. Customers were informed that though the bed exit system will alert at the bed, it may fail to send a remote alert through the nurse call system. The firm's letter states that the risk can be immediately mitigated by changing the nurse call setting from "SideCom" to "With A.C." For detailed instructions, please see "Instructions: Changing the Nurse Call Setting" section of the letter. Customers should also complete the response form and return it to the firm. The latest software (version 1.28.000 or greater) resolves the communication issue and mitigates the potential patient risk. A software update to the latest software is required for affected devices. Once Hill-Rom receives your response form and has confirmed that your device is affected, the firm will contact you to schedule your software update. If you have any questions or would like to proactively schedule your software update, please contact Hill-Rom Technical Support at 1-800-445-3720 (select option 2 and then select option 1) Monday through Friday, 8:00AM 5:00 PM EST.
Propane Leak from Fill Gauge
A fuel leak in the presence of an ignition source increases the risk of a fire.
Dealers will replace the bleed valve on the propane tank, free of charge. Owner notification letters were mailed January 31, 2024. Owners may contact Forest River Customer Service at 1-574-825-6225. Forest River's number for this recall is 225-1696.
Door Windows Incorrectly Labeled/FMVSS 205
An incorrect DOT code mark may result in the window being replaced with an incorrect type of glass, reducing visibility and increasing the risk of a crash.
Nova Bus will inspect the windows and either replace the windows or remove the incorrect marking, free of charge. Owner notification letters were mailed July 19, 2024. Owners may contact Nova Bus customer service at 1-800-350-6682. Nova Bus number for this recall is CR5546.
Overloaded Electrical System May Cause Fire
Overloaded electrical circuits can overheat, increasing the risk of fire.
MAXI-METAL will work with Weldon to update the firmware, free of charge. Owner notification letters were mailed February 22, 2024. Owners may contact MAXI-METAL customer service at 1-418-228-6637.
Verigene Processor SP, Model Numbers 10-0000-07 and 10-0000-07R. Used with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product Usage: IVD sample processor, which utilizes a single-use disposable test consumable and a self-contained Verigene Test Cartridge for each sample tested.
Luminex has determined that three (3) separate test fixtures used by field service engineers to service the VERIGENE SP Processors were procured from unapproved sources and, in some cases, were manufactured using unvalidated processes. These text fixtures were used to calibrate and verify VERIGENESP devices.
On 10/13/2020, the firm sent the following notice: "As part of our corrective action plan, Luminex will be updating software on all VERIGENE SP instruments in the coming weeks, and systematically visiting every VERIGENE customer site to perform a supplemental preventative maintenance on your instruments. We will also likely be sending out a series of Customer Advisory Notifications with additional information on items related to our remediation efforts surrounding the Warning Letter, as well as updates related to other items identified for improved product performance. During this time, you may continue to use your VERIGENE products as directed in the package inserts for each product, or as otherwise directed through further Luminex communications. If you have any question, please do not hesitate to contact Luminex Global Support Services using the contact details below: Luminex Global Support Services 1-877-785-2323 (U.S. and Canada) +1-512-381-4397 (Outside U.S. and Canada) support@luminexcorp.com"
Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q; Fortify ST VR, Model Numbers: CD1241-40 and CD1241-40Q; Fortify Assura VR, Model Numbers: CD1257-40, CD1257-40Q, CD1357-40C, CD1357-40Q; Fortify Assura ST VR, Model Numbers: CD1263-40, CD1263-40Q, CD1363-40C, CD1363-40Q; Fortify DR, Model Numbers: CD2231-40 and CD2231-40Q; Fortify ST DR, Model Numbers: CD2241-40 and CD2241-40Q; Fortify Assura DR, Model Numbers: CD2257-40, CD2257-40Q, CD2357-40C, CD2357-40Q; Fortify Assura ST DR, Model Numbers
The device may exhibit premature battery depletion.
Abbott sent a Field notification letter dated August 28, 2017 to customers of the availability of the new Battery Performance Alert. The letter identified the affected product, problem and actions to be taken. The recalling firm posted a public statement on their website in the Abbott Media Room. The link to the statement is as follows: http://abbott.mediaroom.com/2017-08-29-Abbott-issues-new-updates-for-implanted-cardiac-devices. For questions contact your local Sales Representative or Abbott Technical Services at 1-800-722-3774.
Exterior A-Pillar Trim May Detach
A detached trim piece can fall off the vehicle, becoming a road hazard and increasing the risk of a crash.
Dealers will inspect and replace the A-pillar trim as necessary, free of charge. Owner notification letters were mailed on July 18, 2024. Owners may contact Ford customer service at 1-866-436-7332. Ford's number for this recall is 24S02.