Archive
556 recalls were announced in March 2024.
Of the 556 recalls this month scored against our rubric, 4% are Critical, 27% are Severe.
Which agencies issued them
Big Tex Trailer Manufacturing is recalling 2024 25GN, 25PH, 3XGN, and 3XPH trailers because improperly installed oil seals may leak onto the brake system, increasing crash risk.
Stateside Bead Supply is recalling high-powered 5mm magnetic beads sold online from November 2022 through June 2023 because they violate federal magnet safety regulations and pose an ingestion hazard. If swallowed, the magnets can lodge in the digestive system and cause serious injury or death.
General Motors is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles because front wheel hub bolts may have been over-tightened and damaged during installation.
Chrysler is recalling certain 2024 Pacifica and Voyager vehicles whose windshields may not have been properly bonded, allowing them to detach during a crash. This fails FMVSS 212.
Polaris is recalling about 7,000 Model Year 2022–2023 snowmobiles equipped with PATRIOT BOOST engines because the fuel line between the fuel rails can leak, posing a fire hazard. Consumers should stop using the recalled snowmobiles and contact Polaris for a free repair.
Forias pack and play mattresses sold on Amazon.com from May through August 2023 violate federal crib mattress safety standards and pose a suffocation hazard to infants. The product is missing required warnings and labels.
Micro Bird is recalling one 2019 G5 Transit Bus because a module failure may disable the windshield defrosting system, reducing visibility.
BJ's Wholesale Club is recalling about 90,000 Berkley Jensen Citronella 72-inch Tiki Torches because the torch top can break open or fall off while lit, creating a burn hazard. The company has received nine reports of the top breaking or falling, including two burn injuries.
Chrysler is recalling certain 2022 Jeep Cherokee vehicles because the turn signal self-cancelling feature may not work properly, failing FMVSS 108.
Chrysler is recalling certain 2024 Pacifica and Voyager vehicles because the traction control system does not function while cruise control is activated. A free software update is the remedy.
Micro Bird is recalling 2019 G5 school buses because a module failure may disable the windshield defrosting system, reducing driver visibility.
Pure Brands of California is recalling Purefog High Density Natural Fog Juice Liquid because the product can expire sooner than the printed expiration date, posing a mold-exposure risk to people with compromised immune systems, damaged lungs, or mold allergies.
Reser's Fine Foods is recalling Don Pancho Fiesta 3 Pack Everything Sauce due to potential Listeria monocytogenes contamination from recalled Cotija cheese repackaged into these ready-to-eat products.
Fresh & Ready Foods LLC is recalling Fresh & Ready Chicken Torta Sandwich products (use-by dates 02/03/2024–02/22/2024) due to Listeria monocytogenes contamination. Affected products were distributed to California, Nevada, Utah, and Arizona.
Reser's Fine Foods is recalling HEB Poblano Caesar Dressing due to Listeria monocytogenes contamination from repackaged Cotija cheese. The recall affects 2495 cases distributed across 16 states.
Fresh & Ready Foods LLC recalled Fresh & Ready Ham Torta Sandwich (9 oz) due to possible Listeria monocytogenes contamination. The recall affects products distributed in California, Nevada, Utah, and Arizona with use-by dates February 3–22, 2024.
Stonewall Kitchen is recalling Cinnamon Sugar Doughnut Mix (Gluten Free) with use-by dates of March 9-10, 2025, because units contain undeclared wheat. Consumers with wheat allergies or celiac disease should not consume this product.
Heartland is recalling 10,038 model year 2023-2024 fifth wheels and travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat, increasing the risk of a fire.
Sprig & Sprout Ham Torta Sandwich is being recalled due to potential Listeria monocytogenes contamination. The product was distributed to CA, NV, UT, and AZ with Use By dates from January 27 to February 15, 2024.
Nova Bus is recalling certain 2020-2024 LFS vehicles because the engine coolant return hose may fail, leading to engine shutdowns and increased crash risks.
Dole Fresh Vegetables Inc is recalling Marketside Chopped Salad Kit Bacon Crunch due to potential Listeria monocytogenes contamination. Affected packages have lot codes B020-B036 with production dates from February 5, 2024 through February 21, 2024.
Reser's Fine Foods is recalling Cilantro Lime Crema products sold under Costco and Don Pancho labels due to Listeria monocytogenes contamination. Products were distributed across 16 states.
Reser's Fine Foods is recalling multiple chicken taco kits distributed across 16 states due to potential Listeria monocytogenes contamination in a repackaged cheese ingredient. Consumers should not consume affected products.
Dole Premium Kit Southwest Salad is being recalled due to potential Listeria monocytogenes contamination. Consumers who purchased affected products should not consume them.
Keystone RV Company is recalling various 2021-2024 RV models because the cooktop LED backlight circuit board may overheat and increase the risk of fire.
Fresh & Ready Foods LLC recalls Jack & Olive Ham Torta Sandwich due to Listeria monocytogenes contamination. The product was distributed in California, Nevada, Utah, and Arizona with use-by dates from January 27, 2024 to February 15, 2024.
Reser's Fine Foods is recalling HEB Cilantro Cotija Dressing due to potential Listeria monocytogenes contamination. The dressing was distributed across multiple states in approximately 5,589 cases.
Reser's Fine Foods is recalling Costco Southwest Wrap Kits due to Listeria monocytogenes contamination. The product was distributed across 16 states.
The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.
Dole Chopped Kit Avocado Ranch (UPC 71430000915) is being recalled due to potential contamination with Listeria monocytogenes. The FDA Class I recall affects 50,645 cases distributed across the United States and Canada.
Cruiser RV is recalling 2023-2024 travel trailers and fifth wheels because a faulty LED circuit board in the cooktop may overheat and cause a fire.
Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.
Dole Fresh Vegetables is recalling 50,645 cases of Dole Cajun Ranch Chopped Kit UPC 71430002063 due to potential Listeria monocytogenes contamination. The affected product was distributed in 24 U.S. states and Canada.
PACCAR is recalling certain 2025 Peterbilt and Kenworth trucks because the steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.
Wesco Central Commissary is recalling Wesco mint no-bake cookie bites because they contain undeclared peanut and soy allergens that are not listed on the label. The affected product was distributed in Michigan.
Mack Trucks is recalling 2024-2025 LR natural gas vehicles because a missing fuse may render the methane detector inoperative, increasing the risk of fire or injury.
Smiths Medical Pneupac Plus 300 ventilators may intermittently deliver continuous airflow instead of cycling breaths as designed. This malfunction affects 2,902 units distributed worldwide.
Smiths Medical is recalling paraPAC plus 310 ventilators that may malfunction by delivering continuous gas flow instead of cycling breaths. The defect affects 10,140 units distributed worldwide and prevents proper ventilation.
Neptune's Fix Tianeptine Elixir, distributed nationwide by Super Chill Products, is recalled because it contains tianeptine, a substance not approved by the FDA for any medical use in the United States. Consumers should not use this product.
ARROW International is recalling 1,160,470 QuickFlash radial artery catheterization devices due to a defective guidewire handle that can cause arterial vasospasm and vessel injury.
A vascular guidewire introducer is recalled because internal voids in the hub may prevent proper guidewire passage, potentially delaying surgical procedures.
Bob Evans Original Mashed Potatoes (2 lbs) with UPC 75900005349 from batch KCL1 are being recalled due to potential red plastic contamination. No illnesses have been reported.
Thommen Medical AG is recalling impression coping units because the internal canal depth was not manufactured according to specifications, preventing firm connection to the dental implant. The product was distributed in Ohio and Kentucky.
Ethos Bakery is recalling 4 oz packages of Vegan Snickerdoodles distributed in Washington because the labels do not clearly specify that wheat flour is present, creating a risk for consumers with wheat allergies.
Curaplex Nasal Intubation Kit recalled because the included endotracheal tube holder is incompatible with nasal intubation procedures, preventing practitioners from properly securing the tube.
Mc3 Inc recalls Nautilus ECMO Oxygenator units due to heat exchanger water path restriction that degrades temperature control performance. Inadequate heat transfer may lead to hypothermia risk.
Hikma Pharmaceuticals is recalling Infumorph 200 (morphine sulfate) ampuls because the sterile filter in the carton has an earlier expiration date than the medication, potentially compromising sterility.
Angiodynamics recalls 130 MINI STICK MAX guidewire introducers due to hub voids that may prevent guidewire passage during vascular procedures. No injuries reported.
Sarnova HC is recalling the Curaplex Nasal Intubation Kit because the endotracheal tube holder is incompatible with nasal intubation, preventing practitioners from securing the tube. The recall affects 550 units distributed nationwide.
Preat Corp is recalling 561 units of RP Titanium Abutment Blanks due to a manufacturing defect where the screw seat location may be too high, resulting in shortened screw engagement into the implant.
A batch of I.B.S compression screws may have incorrect dimensions compared to their labels due to a batch mix-up. The 59 affected units were distributed nationwide in Tennessee.
Ethos Bakery is recalling Vegan Pecan Oat Scones distributed in Washington because the product label fails to declare wheat as an allergen, despite wheat flour being present in the product.
Angiodynamics recalls the MINI STICK MAX vascular guidewire introducer due to internal defects in the sheath hub that may prevent guidewire insertion during surgery, potentially requiring equipment exchange.
Angiodynamics recalls approximately 5,840 guidewire introducers with manufacturing defects that may prevent proper guidewire insertion during vascular procedures. The defect could cause procedural delays requiring equipment exchange.
Dole Fresh Vegetables Inc is recalling Dole Premium Kit Endless Summer salad kits due to potential Listeria monocytogenes contamination. Affected products have specific production codes dated February 2024.
Mc3 Inc is recalling 188 Nautilus Smart ECMO modules nationwide due to potential water path restrictions in the heat exchanger that may cause inadequate heat transfer and risk of hypothermia during use.
Abbott's i-STAT Level 1 control device is recalled because a refrigerator temperature excursion on January 8, 2024, could cause incorrect or delayed test results. The walk-in storage unit failed, causing temperatures to fall below the required range of 35.6-46.4°F.
D.O.R.C. Dutch Ophthalmic Research Center is recalling Directional Laser Probes for ophthalmic surgery due to difficulties extending, retracting, and directing the laser fiber. The recall affects 84 units distributed nationwide.
Covidien is recalling Situate Laparotomy Sponges because some packs may contain improperly sterilized units lacking required RF detection features. Non-sterile sponges could cause infection, tissue trauma, and sepsis during surgery.
A Class II medical device recall has been issued for Directional Laser Probes due to potential difficulties extending, retracting, and directing the laser fiber tip. The issue affects 126 units distributed across multiple US states.
ConvaTec is recalling specific lots of EsteemBody Soft Convex Drainable Pouches due to inconsistency in filter weld strength, affecting 6709 units distributed in the US and internationally.
El Chilar ground cinnamon (1.25 oz bags) is being recalled due to elevated levels of lead. Affected products were distributed in Maryland; consumers should not use them.
Baxter Healthcare is recalling HDS Traction Boot II units due to incorrect assembly. The boot key socket locking ridge faces upward, preventing proper attachment to the traction system.
Beckman Coulter recalls Access Total T4 thyroxine assay due to imprecision that may cause erroneous or delayed diagnostic results.
Angiodynamics is recalling MINI STICK MAX guidewire introducers (155 units) due to manufacturing defects in the sheath hub that may prevent guidewire passage.
Eberspacher is recalling Hydronic L-II heaters produced between May 2023 and January 2024 because they may release excessive exhaust gas, posing a risk of smoke poisoning or fire.
Eugia US LLC is recalling 43,920 vials of Nicardipine Hydrochloride Injection nationwide due to failure to meet organic impurity specifications. No illnesses have been reported.
Albertsons is recalling Signature Select, Athens, and Cal Pia brand Bread Butter White Bread due to possible metal and plastic shavings in the product. The recall affects approximately 13,550 units distributed in California and Nevada.
A precision component in Think Surgical's TMINI robotic knee system may bind due to insufficient clearance. The binding could occur during surgical drilling.
D.O.R.C. recalls 78 directional laser probes with Alcon/Lumenis connectors due to difficulties extending, retracting, or directing the laser fiber. The Class II recall affects units distributed across multiple U.S. states and Puerto Rico.
Siemens is recalling its DCA HbA1c Reagent Kit because the device displays falsely elevated readings without alerting the user. This could lead to incorrect patient management of glucose levels.
Novitium Pharma LLC recalls Digoxin 125mcg tablets nationwide due to cross contamination with mycophenolate mofetil, a different medication. Patients receiving contaminated tablets could experience unintended drug effects.
Eugia US LLC is recalling Nicardipine Hydrochloride Injection nationwide due to failed impurity specifications. The 335,940 affected vials contain organic impurities exceeding acceptable standards.
Angiodynamics vascular guidewire introducers (600 units) may have internal defects preventing proper function during surgery. Defects could cause procedure delays and require device exchange.
In2Bones, SAS is recalling I.B.S Compression screws due to a batch mix-up. Affected screws may have different lengths than indicated on their labels, creating a risk of improper surgical implantation.
Angiodynamics recalls MINI STICK MAX vascular guidewire introducers due to internal lumen defects that may prevent the guidewire from passing through during surgery, potentially requiring device exchange.
La Fiesta ground cinnamon (Canela Molida) is being recalled due to elevated lead levels. Affected products are 0.87oz bags with lot code 25033, distributed to retailers in California, Arizona, Washington, and Texas.
Angiodynamics is recalling 58 units of its MINI STICK MAX guidewire introducer due to voids in the internal lumen that may prevent proper guidewire passage. Users may experience procedural delay requiring device exchange.
Medtronic is recalling Abre Venous Self-expanding Stent Systems due to a potential for sterile package breach. The recalled systems consist of three product numbers totaling 65 units distributed worldwide. No injuries have been reported.
McKesson recalls Abbott Rapid Dx pregnancy test control sets due to a refrigerator temperature excursion that could cause inaccurate or delayed test results.
Angiodynamics is recalling 39 units of MINI STICK MAX vascular guidewire introducers due to voids in the sheath hub that may prevent guidewire passage during surgery, potentially delaying the procedure.
Natus Neurology is recalling TENSIVE Conductive Adhesive Gel (Lot A0623009) after complaints of improper thickness, discoloration, and in one case, patient skin irritation following use.
Medtronic is recalling 4,343 units of DLP Vessel Cannula (Model REF 30000) due to incorrect labeling on three manufactured lots distributed globally.
Angiodynamics is recalling MINI STICK MAX guidewire introducer sheaths due to manufacturing defects that may prevent guidewire passage. The defect may cause procedural delays requiring equipment exchange during vascular interventions.
Randox Laboratories is recalling 1,764 units of Liquid Protein Calibrators used in immunoassays due to realignment of C3 and Haptoglobin to the correct reference material standard. Distribution was limited to seven U.S. states.
Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.
Landauer is permanently discontinuing the microStar Reader medical dosimetry system. The company is removing product documentation references and discontinuing use with medical dosimeters.
Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.
A Sekisui Diagnostics control kit for bacterial vaginosis testing was recalled after exposure to temperatures below the validated storage range for up to 60 minutes due to refrigerator mechanical failure.
Angiodynamics is recalling 5,176 units of MINI STICK MAX guidewires due to manufacturing voids that prevent passage through the introducer during surgery. Surgeons may need to exchange the sheath to complete procedures.
Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.
Angiodynamics is recalling 65 units of its MINI STICK MAX guidewire introducer sheath due to manufacturing defects that may prevent guidewires from passing through during surgical procedures.
Angiodynamics recalls MINI STICK MAX guidewire introducer devices due to manufacturing defects in the internal lumen that may prevent guidewire passage and delay surgical procedures.
Angiodynamics is recalling certain MINI STICK MAX vascular guidewire introducer sheaths due to internal voids that may prevent guidewire passage during surgery, potentially causing procedural delays.
Angiodynamics is recalling 959 units of MINI STICK MAX guidewire introducers due to voids in the sheath hub that may prevent proper guidewire placement. Users may experience procedure delays and need to exchange equipment.
Doosan is recalling 2015-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, potentially disabling brakes.
Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because a 12-volt ground connection may overheat, increasing the risk of fire or loss of drive power.
Ford is recalling 2023-2024 Transit vehicles with the Trail package because tires may contact the wheel arch liner, risking tire damage and loss of control.
Volkswagen Group of America is recalling 2022-2023 Audi E-Tron GT and RS E-Tron GT vehicles because a high-voltage battery short circuit could cause a fire.
Volkswagen is recalling certain 2022-2024 Audi RS e-tron GT and e-tron GT vehicles because the high-voltage battery may experience a short circuit within the battery modules.
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