FDA•MODERATE
BioFire Joint Infection Panel
BioFire is recalling the Joint Infection (JI) Panel due to contamination that may cause false positive test results.
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All Recalls
Back to home ←- Device RecallFDA•MODERATEMint Lesion Software
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient information linking.
FDA•MODERATEOne Step 10A in vitro diagnostic testOne Step 10A in vitro diagnostic test recalled for lack of FDA clearance.
7 products
FDA•MODERATEBiofire Spotfire Respiratory/Sore Throat PanelBioFire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.
FDA•MODERATEDEX Ophthalmic Tissue ForcepsKatalyst Surgical recalls DEX Ophthalmic Tissue Forceps, model DVF4005-23, due to IFU corrective action.
12 products
NHTSA•MODERATEMicro Bird G5 and MB II School Bus Drive Belt PulleyMicro Bird recalls 2023–2026 G5 and 2024 MB II school buses; drive belt pulley may damage oil lines and cause fire risk.
NHTSA•MODERATEMicro Bird G5 Transit Bus Drive Belt PulleyMicro Bird recalls 2023–2025 G5 transit buses; drive belt pulley may damage oil lines and cause fire risk.
FDA•CRITICALJOHN B SANFILIPPO & SONS: 6 productsJohn B. Sanfilippo recalls nut mixes over Salmonella risk.
6 products
FDA•MODERATEWoodstock Organic Shelled EdamameWoodstock Organic Shelled Edamame recalled over possible metal pieces.
FDA•MODERATEOctreotide Acetate for Injectable SuspensionTeva is recalling Octreotide Acetate 30 mg injection kits due to a lack of assurance of sterility.
2 products
FDA•MODERATEEnalapril Maleate Tablets, USP 20 mgRising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution due to a lack of assurance of sterility and potential product contamination.
2 products
NHTSA•MODERATETesla Model 3, Model Y, Model S, Model X Rearview CameraTesla recalls Model 3, Y, S, X vehicles with delayed rearview camera image in reverse (software 2026.8.6).
NHTSA•MODERATEWinnebago Solis Liquid Propane HoseWinnebago is recalling 2026–2027 Solis RVs; LP hose may be incorrectly routed over exhaust heat shield, risking fire.
NHTSA•MODERATE2025 Utilimaster Velocity Cargo Capacity LabelShyft is recalling 2025 Utilimaster Velocity vehicles with incorrect cargo capacity labels.
FDA•CRITICALUtz Quality Foods: Zapp's and Dirty Potato ChipsUtz is recalling Zapp's and Dirty potato chips in several varieties for possible Salmonella contamination.
6 products
FDA•MODERATEDELFLEX Peritoneal Dialysis SolutionFresenius recalls DELFLEX dialysis solution due to potential bag leaks compromising sterility.
2 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta recalls Duloxetine 30 mg capsules over nitrosamine impurity above FDA limit.
3 products
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators serviced without proper performance inspections, potentially delaying therapy.
NHTSA•MODERATE2026 Toyota 4Runner Load Capacity Label2026 Toyota 4Runner recalled for incorrect load capacity label that may lead to improper loading.
FDA•MODERATESecond Nature Keto Crunch Smart MixSecond Nature recalls Keto Crunch Smart Mix 10 oz pouches due to undeclared cashews, pistachios, and dried cherries.
FDA•LOWBuspirone Hydrochloride TabletsUnichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the Ultraview SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEProdisc C SK Cervical Disc ImplantCentinel Spine recalls Prodisc C SK cervical disc implants due to labeling mix-up (5mm/6mm).
2 products
FDA•CRITICALCook Centimeter Sizing CatheterCook recalls Centimeter Sizing Catheter (RPN N5.0-35-100-P-10S-PIG-CSC-20) over marker band cracking risk.
3 products
FDA•MODERATEBoston Scientific LUX-DX II Arrhythmia DetectorBoston Scientific recalls LUX-DX II Arrhythmia Detector (M302) with LATITUDE DRAGON US Server (6460) over missing PVC Burden and Bradyarrhythmia monitoring.
2 products
FDA•MODERATEERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical recalls ERBEFLO CleverCap CO2 tubing/cap sets due to risk of water aspiration and respiratory failure.
3 products- Device RecallFDA•MODERATEda Vinci Surgical System Universal Surgical Manipulator
Intuitive Surgical is recalling the USM arm sub-assembly for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products 
FDA•CRITICALIntuitive SureForm 30 Gray ReloadsIntuitive is recalling SureForm 30 Gray stapler reloads due to the risk of an incomplete staple line during surgical procedures.
NHTSA•MODERATEMercedes-Benz Infotainment Control UnitMercedes-Benz is recalling 2024–2026 AMG GT, C-Class, E-Class, SL, CLE, and GLC vehicles; infotainment unit may reset and blank the instrument panel display.
NHTSA•MODERATERam ProMaster Rear Bench Seat LegsBraun is recalling 2026 Ram ProMaster vehicles with rear bench seats missing two of four legs.
NHTSA•MODERATENew Flyer XE40 Speedometer IlluminationNew Flyer is recalling 2022 XE40 transit buses with speedometers that may not illuminate with headlights on.
NHTSA•MODERATEMercedes-Benz CLA 350 4MATIC and CLA 250+ Front Passenger Seat BeltMercedes-Benz recalls 2026 CLA 350 4MATIC and CLA 250+ front passenger seat belts that may remain locked and cannot extend.
- Equipment RecallNHTSA•MODERATEWaymo 5th and 6th Generation Automated Driving System
Waymo recalls 5th and 6th Gen ADS software that may drive vehicles into standing water on high-speed roads.
FDA•MODERATEMy Mochi Strawberry Non-Dairy Frozen DessertMy Mochi Strawberry Non-Dairy Frozen Dessert recalled due to foreign object in container.
FDA•MODERATECalypso Tropic Tango LemonadeCalypso Tropic Tango Lemonade recalled for undeclared Yellow No. 5.
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•MODERATEMedline Universal Central/Art Line Insertion KitMedline recalls kits with Webcol Alcohol Prep Pads due to possible non-sterility and contamination risk.
10 products
NHTSA•MODERATEGrand Design Lineage Seat BaseGrand Design is recalling 2025–2026 Lineage RVs with improperly tightened driver and passenger seat bases that may move in a crash.
- NHTSA•MODERATEGrand Design Lineage Solar Panel
Grand Design is recalling 2025–2026 Lineage RVs; solar panels may detach due to adhesive failure.
NHTSA•MODERATENova Bus LFS Transit Bus Control UnitNova Bus is recalling 2022–2023 LFS transit buses; telemetry control unit may shut down and cause loss of drive power.
FDA•MODERATEAlendronate Sodium Oral Solution 70 mg/75 mLHikma is recalling Alendronate Sodium Oral Solution 70 mg/75 mL (NDC 0054-0282-59) due to out-of-specification assay results.
FDA•MODERATEImmy Myco DDR Trident Neutralization Buffer BImmuno-Mycologics is recalling Myco DDR Trident Neutralization Buffer B due to potential contamination.
FDA•MODERATEATTUNE Revision Hinge FemoralDepuy Synthes recalls ATTUNE Revision Hinge Femoral over packaging adhesion that may compromise sterility.
9 products
FDA•MODERATEepoc BGEM BUN Test CardSiemens is recalling epoc BGEM BUN Test Cards due to inaccurate pH and mTCO2 results that could lead to improper patient treatment.
FDA•MODERATEBD GasPak EZ CO2 Pouch SystemBD recalls GasPak EZ CO2 and Campy pouch systems over low CO2 output.
2 products
FDA•MODERATEPhilips Bridge Prep KitMerit Medical recalls Philips Bridge Prep Kit (REF K12-09098B) over catheter resistance on guidewire.
4 products
FDA•MODERATEi-STAT EG7+ CartridgeAbbott recalls i-STAT EG7+ cartridges (03P76-25) over inaccurate PCO2/pH results.
3 products
FDA•MODERATELeksell Vantage Arc SystemElekta is recalling the Leksell Vantage Arc System due to a risk of coordinate shifting caused by faulty locking mechanisms.
FDA•LOWPALAMIX uno Mixing UnitHeraeus recalls PALAMIX uno mixing units: mixing rod may loosen in units over 17 months old; shelf life reduced to 1.5 years.
2 products