Archive
677 recalls were announced in February 2024.
Of the 677 recalls this month scored against our rubric, 3% are Critical, 24% are Severe.
Which agencies issued them
Mennel Milling Company is recalling approximately 2.6 million pounds of bagel flour distributed in six states due to potential contamination with metal, wood, gasket material, and sifter balls.
Bestco LLC is recalling Equate Cherry Cough Drops nationwide due to potential glass and silicone particulates from manufacturing deviations. Affected products are 30-drop and 160-drop bags expiring December 31, 2026.
Country Corner Dairy is recalling Yellow Colby Cheese distributed in Maryland and Virginia due to insufficient pasteurization during manufacturing.
Country Corner Dairy is recalling Yellow Cheddar Cheese due to lack of proper pasteurization. The product was distributed in Maryland and Virginia and may pose a food safety risk.
Fortune cookies manufactured by New World Company are being recalled due to undeclared soy allergen. Consumers with soy allergies should not consume the product.
Bestco LLC is recalling Family Wellness Cherry Cough Drops nationwide due to potential glass and silicone particulates found during manufacturing. Consumers should stop use immediately.
The framegrabber card in Philips Azurion interventional X-ray systems may fail to display diagnostic images properly, potentially delaying procedures.
Mallinckrodt recalls TERLIVAZ (terlipressin) injection due to temperature excursion during shipping. A cGMP deviation may compromise drug stability.
M&P Production LTD is recalling raw lamb and beef samsa products because they contain sesame seeds, a known allergen, that are not declared on the label.
Patterson Procedure Earloop Masks (ASTM Level 3, blue) are being recalled because units were produced on non-validated equipment. The recall affects 180 cases with lot numbers 2339 and 2342, distributed across six states.
Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.
Baxter Healthcare is recalling 13,000 bags of norepinephrine bitartrate injection due to an overwrap label incorrectly showing 4 mg/250 mL concentration, while the primary bag label correctly shows the actual 8 mg/250 mL strength.
Lupin Pharmaceuticals recalls Voriconazole for Oral Suspension (40mg/mL) due to missing or incorrect package inserts on affected batches distributed in Ohio, Illinois, and New Jersey.
CABTREO acne medication was stored outside refrigeration requirements. The recalled lot was kept at room temperature instead of required refrigerated conditions.
Micro Labs Limited is recalling 24,768 bottles of Clobazam 10mg tablets nationwide due to out-of-specification residual solvents. Patients should contact their healthcare provider for guidance.
Synapse Cardiology PACS software versions 7.0–7.3.0 may calculate left ventricle mass incorrectly, potentially leading to misdiagnosis or wrong treatment plans. Thirteen units have been distributed in the US and Israel.
Olympus Corporation of the Americas is recalling ESG PK Cutting Forceps because the jaw may fracture during pre-procedure inspection or during the procedure, posing a potential injury risk.
A framegrabber card malfunction in Philips Allura Xper interventional X-ray systems may cause display failures, preventing proper visualization of medical images and delaying procedures.
FUJIFILM Synapse CV 6 medical imaging software may incorrectly calculate left ventricle mass measurements. If used for diagnosis, this calculation error could lead to patient misdiagnosis and incorrect treatment, potentially causing long-term health consequences.
IonoStar Plus dental cement capsules contain an incorrect plunger due to a manufacturing error. The defect prevents proper curing of the cement, making the product unsuitable for use.
Philips Allura Xper fluoroscopic X-ray systems may experience memory module failures that cause the system to stop functioning and prevent imaging. This malfunction could delay critical medical procedures.
Philips has recalled certain Allura Xper interventional X-ray systems because the disk bay component may fail, potentially preventing system operation and imaging procedures.
The OPTIMIZER model CCM X11 implantable pulse generator may incorrectly detect a charging error and cease delivering cardiac therapy, potentially causing patients to experience heart failure symptoms. A total of 1,469 units are affected.
Boston Scientific is recalling EndoVive Replacement Button Kits due to sizing mislabeling that could cause undersizing and serious complications including tissue damage and sepsis.
Medline is recalling 1.3 million units of bleach germicidal wipes due to stability concerns. Products labeled for 24-month shelf life are only safe and effective for 12 months.
Pure Care Foaming Mint Hand Sanitizer has been voluntarily recalled due to manufacturing process deviations. The product was distributed to accounts in North Carolina and Michigan.
Amneal Pharmaceuticals is recalling 46,037 bottles of Oseltamivir Phosphate Oral Suspension due to failed quality test results showing impurities and degradation. The FDA classified this as a Class II recall affecting nationwide distribution.
W&H Surgical handpiece S-12 devices were incorrectly laser marked with '1:1' instead of the correct '1:2' during production. 160 units are affected.
Mennel Milling Company is recalling approximately 2.6 million pounds of bulk milling product due to potential contamination with foreign materials including metal, wood, and gasket material distributed across six states.
Meta Psyllium Fiber Capsules in 100 and 160 count bottles are being recalled because the product labeling is illegible. Approximately 21,428 cases were distributed across most US states.
Nissan is recalling certain 2023-2024 vehicles, including the Rogue, due to a manufacturing issue that may allow the driver's air bag inflator to absorb moisture and deploy improperly.
Toyota is recalling certain 2022-2023 Tacoma trucks because the rear axle shaft may separate from the axle housing due to debris causing improperly secured fasteners, increasing the risk of a crash.
Tesla is recalling certain 2013-2022 Model S, X, 3, and Y vehicles because a factory reset can mute the Pedestrian Warning System sounds, increasing crash risk for pedestrians.
USDA FSIS issued a public health alert for Nurture Life Chicken Parm with Super Veggie Spaghetti due to an undeclared egg allergen. Consumers with egg allergies should not consume the product.
Lippert is recalling MTP 20K Surge Brake Couplers with part number 2023050981 because incorrect labels may allow the brake system to be overloaded.
Daimler Coaches is recalling 2022-2024 Mercedes-Benz Tourrider vehicles because the roof hatch handle may break, potentially delaying emergency exits.
Pleasant Valley Teardrop Trailers is recalling 2023-2024 nuCamp truck campers with Lithium Upgrades because an incorrect battery disconnect switch may overheat and cause a fire.
LiveWire is recalling certain 2024 S2 Del Mar motorcycles because the Vehicle Supervisory Control software may initiate a powertrain shutdown. 523 units are affected.
Kia is recalling 2020 Telluride vehicles because high beam headlights may fail, reducing visibility and increasing crash risk.
Pierce Manufacturing is recalling 2023-2024 Commercial Chassis because a firmware defect in specific multiplex nodes can cause electrical circuits to overheat and potentially start a fire.
Ford is recalling EcoSport rear seat covers that may prevent air bags from deploying correctly, increasing injury risk in a crash.
Forest River is recalling 2024 Elkhart ELKC transit buses because unsecured brake lines may damage and cause loss of brake pressure.
Ford is recalling certain 2023-2024 F-650 and F-750 vehicles because the parking brake may malfunction and allow the lever to be released without pressing the release button.
Ford is recalling 2023 F-150 Lightning vehicles because loose battery fasteners may cause electrical arcing, increasing the risk of fire or loss of drive power.
PACCAR is recalling certain 2009-2024 Kenworth trucks because the air tanks have an insufficient volume of air for the brake system, which can reduce braking performance.
Ford is recalling certain 2022-2023 Maverick Hybrid vehicles because the instrument panel cluster may not properly illuminate warning lights or gauges. 62,813 units affected.
Ford is recalling certain 2023-2024 Bronco and Bronco Heritage vehicles because rear quarter glass panels may have been improperly installed to the hard top and can detach.
Hyundai is recalling 2015-2016 Elantra vehicles because a damaged trunk latch may prevent opening from the inside, potentially trapping occupants.
BMW is recalling certain 2024 XM vehicles because the tailgate panel may detach from the mounting structure due to improper adhesive bonding during manufacturing. 267 units affected.
BMW is recalling certain 2024 i4 xDrive40, i4 M50 and i5 eDrive40 vehicles because the high-voltage battery module may contain insufficient weld seams, which can cause overheating.
Forest River is recalling certain 2024 IBEX and No Boundaries travel trailers because the recessed space heaters may have been installed too close to the ceiling. 98 units affected.
Daimler Coaches is recalling 2022-2024 Mercedes-Benz Tourrider vehicles equipped with BraunAbility wheelchair lifts because the outer barrier may deploy unexpectedly.
BMW is recalling certain 2024 X5 and X7 vehicles because the instrument panel may not have been manufactured properly, which can result in improper airbag deployment or panel separation.
Chrysler is recalling certain 2021-2023 Jeep Grand Cherokee L and 2022-2023 Grand Cherokee vehicles because the upper control arm ball joint and steering knuckle may separate. 338,238 units affected.
Machir LLC recalled about 24,820 biometric personal safes because the biometric lock can fail and allow unauthorized access. The firm received 15 reports of the lock failing to secure safes, posing a serious injury hazard and risk of death if firearms are stored inside.
Bulldog Cases is recalling about 33,500 Magnum Biometric Pistol Vaults because the biometric lock can fail and be opened by unauthorized users, creating a serious injury hazard and risk of death when firearms are stored in the safe.
The CPSC is recalling about 2,200 MouTec brand biometric firearm safes because the biometric lock can be opened by unauthorized users, posing a serious injury hazard and risk of death. One incident involved a 6-year-old opening the safe, though no injuries have been reported.
Chrysler is recalling certain 2024 Jeep Grand Cherokee vehicles because an improperly machined steering knuckle may separate, causing the wheel to fall outward. 250 units affected.
About 230 JURLEA area rugs sold on Amazon violate federal flammability regulations and pose a fire hazard. No injuries have been reported. Consumers should stop using the rugs and contact the distributor for a refund.
Jaguar is recalling certain 2021-2024 I-Pace vehicles because the turn signal flash rate will not change to warn the driver that a turn signal has stopped working, failing FMVSS 108.
Worthington Enterprises is recalling about 146,160 EVAS 20-lb propane exchange cylinders that could leak gas and pose a fire hazard. Consumers should stop using them immediately and return them to AmeriGas for free replacement.
The CPSC has recalled Spring Spirit and Biloban pack and play mattresses sold on Amazon.com due to a suffocation hazard to infants. The mattresses violate federal safety regulations and lack required warnings and labels.
IKEA is recalling about 22,600 ÅSKSTORM 40W USB Chargers because the cable can become damaged or break over time, creating burn and electric shock hazards. Consumers should stop using the chargers immediately and return them to any IKEA store for a full refund.
About 60,000 Awesafe biometric gun safes can fail to lock, allowing unauthorized users to open them. No injuries reported, but consumers should immediately stop using the biometric feature and use the key instead until they receive a free replacement.
Cascade Designs is recalling select MSR camping cooking pots because the handle can detach or become loose, spilling hot food and liquids and causing burn or scald injuries. The company has received 22 reports of handle problems, including two burn injuries.
Chrysler is recalling certain 2022-2023 Ram ProMaster vehicles because the driver seat belt warning light and audible chime may not activate as intended, failing FMVSS 208.
Chrysler is recalling certain 2023-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because the driver may be unable to quickly activate the high beams in AUTO, failing FMVSS 108.
GM is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles because the front camera module may falsely detect an obstacle and engage automatic emergency braking unexpectedly.
Polaris is recalling Model Year 2022–2024 MATRYX snowmobiles with PATRIOT 650 and 850 engines because the primary clutch can fail and separate from the vehicle, creating an injury hazard. Polaris has received 109 reports of clutch failure, including one incident resulting in a laceration injury.
Magik & Kover Pack and Play Mattresses sold on Amazon are being recalled because they violate federal safety regulations for crib mattresses and pose a suffocation hazard to infants. Consumers should immediately stop using the mattresses and contact the company for a refund.
Byrne Dairy, Inc is recalling Mighty Fine Chocolate Ice Cream because it contains undeclared peanuts. Consumers with peanut allergies should not consume this product.
Fresh Express Kit Salsa! Ensalada salad kits are recalled for potential Listeria monocytogenes contamination in the cheese condiment. The affected 12.1 oz bags were distributed to AL, FL, GA, CA, UT, WA, and Canada.
Fresh Express Incorporated is recalling Chopped Salad Kit Southwest products due to potential Listeria monocytogenes contamination in the cheese condiment pack. Consumers should not consume the product.
GE Healthcare incubator hoods can appear closed but may not be properly latched, posing a fall risk if patients impact an unsecured panel.
GE Healthcare incubators have defective bedside panels that may appear closed but not be properly latched, creating a patient fall risk when the panels disengage upon impact.
Al Amir Fresh Foods Classic Hummus Creamy Garbanzo is recalled because it contains sesame (tahini) but the label does not declare sesame as an allergen. Consumers with sesame allergies may experience allergic reactions.
GE Healthcare Lullaby Incubator bedside panels and portholes may appear closed but not be properly latched. If impacted, these panels can disengage and fall open, creating a fall risk for patients.
GE Healthcare is recalling 1,410 neonatal incubators worldwide because bedside panels and portholes can appear closed while not properly latched. If impacted, they may fall open and fail to protect patients from falls.
Hans Kissle Company is recalling Mexican Style Quinoa Salad due to undeclared soy and egg allergens. The product was distributed in the Northeast and may pose serious risk to consumers with allergies.
U.S. Tov, Inc. is recalling Dragonfly Jelly Bar Handbags and Backpacks due to a potential choking hazard from konjac. The products were distributed nationwide.
Impella cardiac catheters are being recalled due to risk of left ventricle perforation during operator use. The FDA has classified this Class I recall affecting 91,914 units worldwide.
GE Healthcare is recalling neonatal incubators because the bedside panel can appear closed while unlatched. Impact could cause it to fall open, risking patient injury.
Al Amir Fresh Foods Harissa Spicy Hummus With a Kick is being recalled due to an undeclared sesame allergen. The product declares tahini but not sesame, which could cause serious allergic reactions in people with sesame sensitivity.
Utz Wavy Originals Potato Chips (2.75 oz) distributed in New York may contain undeclared milk and could pose a risk to people with milk allergies.
The bedside panel on GE Healthcare Care Plus incubators may appear closed while unlatched. If impacted, the panel can fall open, exposing patients to injury risk.
Dynabook Americas is recalling about 15.5 million Toshiba laptop AC adapters that can overheat and spark, posing burn and fire hazards. The firm has received 679 reports of overheating or fire, including 43 reports of minor burn injuries.
Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant is recalled for undeclared sesame. The product contains tahini but the label does not list sesame as an ingredient, posing a risk to consumers with sesame allergies.
Stryker, Inc. is recalling 63 units of the Trevo Trak 21 Microcatheter because the device instructions contain an intended use that has not been evaluated by the FDA.
Abiomed is adding safety warnings to Instructions for Use for all Impella catheter models to prevent fibers from entering the device, which could result in reduced flow. The warning applies to all Impella models distributed worldwide.
Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) negative control is contaminated with Norovirus. Users testing this control will incorrectly receive positive Norovirus results.
HeartSine samaritan PAD defibrillators shipped in test configuration may have incorrect CPR timing and delayed or no therapy delivery in cardiac events. Users should stop using affected units and contact the manufacturer.
The Philips CombiDiagnost R90 fluoroscopy device may display a previous patient's radiography images during an examination, risking privacy violation and diagnostic errors in 86 affected units.
Al Amir Fresh Foods Tzatziki Cucumber Yogurt is recalled due to undeclared milk on the label. The product contains sour cream and yogurt but does not declare milk as an ingredient, posing a risk to milk-allergic consumers.
Philips CombiDiagnost R90 fluoroscopy systems may display a previous patient's images during radiography examination, potentially showing different image content, format, and size that could affect imaging accuracy.
Zimmer Surgical Inc. is recalling 3:1 Dermacarrier skin graft carriers due to a manufacturing defect where the ridge pattern is 1.5:1 instead of 3:1, potentially causing tissue damage or additional grafting.
IntegraDose Compounding Services is recalling Vasopressin injectable syringes because the medication may lose potency before its labeled expiration date, potentially leaving patients with reduced doses.
Philips is recalling 20 ProxiDiagnost radiography/fluoroscopy systems due to two issues: potential display of previous patient images when scanning new patients, and a security vulnerability allowing unauthorized data access. No injuries have been reported.
Spencer is recalling 2020 Pumper fire trucks because a firmware defect in Weldon nodes may cause overloaded electrical circuits, increasing the risk of fire.
Maquet is recalling an HLS Set Advanced 5.0 component used in CARDIOHELP heart-lung machines due to a compromised sterile barrier that may cause infection. The recall affects 6,657 US units.
Toyota is recalling certain Lexus and Toyota Mirai vehicles with a Panoramic View Monitor because the rearview camera image may not display immediately after shifting into reverse.
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