The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

14801–14825 of 53092

  • HighFDA (Drugs)·D-0103-2023·2023-01-18

    QuadMix Plus Injectable Medication Recalled for Lack of Sterility Assurance

    Northern VA Compounders is recalling QuadMix Plus injectable medication due to lack of assurance of sterility. The recall affects 78 vials distributed nationwide.

    Product
    QuadMix Plus (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine) 20mcg/30mg/2mg/0.2mg/mL INJECTABLE, packaged in 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0941-2023·2023-01-18

    HCT MAX BARRIER PICC Insertion Tray Recalled for Potential Sterility Breach

    Stradis Healthcare is recalling HCT MAX BARRIER PICC Insertion Trays due to potential pinhole leaks in the outer bag that may compromise sterility. No illnesses have been reported, but affected healthcare facilities should immediately discontinue use of the affected lot.

    Product
    HCT MAX BARRIER PICC INSERTION TRAY 12 per case. Distributed by Health Care Technology
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V010000·2023-01-17

    Chrysler Pacifica Electrical Short Circuit May Cause Engine Shutdown

    Chrysler is recalling certain 2017-2023 Pacifica Plug-In Hybrid vehicles due to a wiring connector short circuit that may cause unexpected engine shutdown and loss of drive power.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V007000·2023-01-16

    Peterbilt 579 and Kenworth T680 electronic stability control software defect

    PACCAR is recalling approximately 46 Peterbilt 579 (2022-2023) and Kenworth T680 (2023) vehicles with faulty electronic stability control software that may underestimate vehicle mass, reducing crash prevention performance. Dealers will provide a free software update.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E002000·2023-01-16

    Suburban SDS2 Cooktops Recalled for Potential Gas Leak and Fire Risk

    Suburban is recalling SDS2 2-Burner Drop-in Cooktops because internal aluminum burner tubes may fracture, causing a gas leak that could lead to fire.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V006000·2023-01-16

    2023 Triumph Speed Triple RR Radiator Fan Overheat Recall

    Triumph is recalling 2022-2023 Speed Triple RR and RS motorcycles because the radiator fan may overheat and fail, causing hot coolant to leak or spray and increasing the risk of injury and crash.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE RS, SPEED TRIPLE RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V005000·2023-01-13

    ABS Remorques semi-trailers recalled for coupling plate deterioration

    ABS Remorques is recalling 2014-2023 RC, WC, LRC, and LWC semi-trailers due to coupling plate deterioration that may cause king pin failure and trailer detachment. Detached trailers cannot be controlled and may crash or obstruct traffic.

    Product
    ABS REMORQUES — ABS REMORQUES LWC, LRC, WC, RC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E004000·2023-01-13

    Comoto Recalls Bilt Vertex Helmets for Safety Standard Non-Compliance

    Comoto Holdings is recalling specific Bilt Vertex motorcycle helmets because they may lack proper retention and penetration protection, increasing crash injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23721·2023-01-12

    LG 86-inch Smart Televisions Recalled for Tip-Over and Entrapment Hazards

    LG is recalling about 52,000 of its 86-inch smart televisions with stands because the stand can become unstable, creating tip-over and entrapment hazards that can result in injuries or death. Consumers should immediately detach the stands and place the TVs in a safe location away from children.

    Product
    LG 86-inch smart televisions and stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23090·2023-01-12

    2019-2021 Honda Talon 1000 ROVs Recalled for Engine Failure and Crash Risk

    American Honda is expanding its recall of 2019-2021 Honda Talon 1000 recreational off-highway vehicles because a loose intake funnel band screw can enter the engine, cause sudden failure, and result in loss of control and crashes.

    Product
    2019-2021 Honda Talon 1000 ROVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V003000·2023-01-12

    Altec Recalls 2022 Digger Derrick Vehicles Due to Incorrect Bolt

    Altec is recalling 2022 Digger Derrick vehicles because an incorrect bolt may have been used on the derrick rotation bearing, increasing the risk of injury.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23722·2023-01-12

    MI Windows and Doors 1620 Vinyl Single-Hung Impact Windows Recall

    MI Windows and Doors is recalling about 25,000 model 1620 vinyl single-hung impact windows with window opening control devices due to a defective tilt latch that can cause the control devices to malfunction, posing fall and serious injury hazards.

    Product
    1620 vinyl single-hung impact windows with window opening control devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2023·2023-01-11

    Steris VERIFY Steam Test Pack biological indicators show inconsistent performance

    Steris Corporation is recalling VERIFY Steam Test Pack biological indicators (lot #230613) due to inconsistent performance in promoting spore growth. When used to monitor sterilization, some indicators may not show growth even if the sterilization cycle was ineffective, creating false assurance of sterility.

    Product
    VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended for use in installation testing and routine monitoring of steam and ethylene oxide sterilization processes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0130-2023·2023-01-11

    Epi-Caine Intraocular Injection Recalled Due to Raw Material Discoloration

    Pine Pharmaceuticals is recalling Epi-Caine intraocular injection (11,453 vials nationwide) due to discoloration in raw material used for compounding, a manufacturing quality control failure.

    Product
    Epi-Caine, Epinephrine 0.025% Lidocaine HCL 0.75% Solution for Intraocular Injection, 1 ml, Single Dose Vial, Compounded by Pine Pharmaceuticals, 355 Riverwalk Pkwy, Tonawanda, NY 14150. NDC 69194-0948-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0871-2023·2023-01-11

    Medical Diagnostic Device Recalled Due to Temperature and Time Excursions

    Biomerieux Inc. is recalling PPM LOMBARD diagnostic products due to storage temperature and time conditions being exceeded during distribution, which compromises the product's guaranteed performance.

    Product
    PPM LOMBARD PRODUCTS CT&IR&DB-TSA + L & P80 10PLT, CATALOG C6045-IR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0799-2023·2023-01-11

    VIDAS Salmonella Diagnostic Test Kits Recalled Due to Storage Damage

    Biomerieux Inc. is recalling 15 units of VIDAS VIDAS Salmonella 60T diagnostic test kits (Catalog 30702) because storage conditions exceeded acceptable temperature and time parameters. The affected test kits may not perform reliably.

    Product
    VIDAS CLINICAL VIDAS SALMONELLA 60T, CATALOG 30702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0846-2023·2023-01-11

    ETEST Antibiotic Susceptibility Test Kit Recalled for Storage Degradation

    Biomerieux Inc recalled ETEST antibiotic susceptibility test kits from batch 1009384490 due to storage conditions exceeding safe temperature and time parameters, potentially affecting test accuracy.

    Product
    ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0876-2023·2023-01-11

    PPM Lombard Phosphate Buffer Recall Due to Temperature Exposure

    Biomerieux Inc is recalling PPM Lombard Phosphate Buffer products due to temperature and time exposure during storage or transport that may have compromised product performance.

    Product
    PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0795-2023·2023-01-11

    VIDAS Varicel Zoster IGG 60T Recalled Due to Storage Condition Excursion

    Biomerieux Inc is recalling VIDAS Varicel Zoster IGG 60T (Catalog 30217, Batch 229478) due to storage temperature and time exceedance. The recalled units cannot be guaranteed to perform accurately.

    Product
    VIDAS CLINICALVIDAS VARICEL. ZOSTER IGG 60 T, CATALOG 30217
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0801-2023·2023-01-11

    Medical device diagnostic plates recalled for storage condition violations

    Biomerieux Inc is recalling PPM Clinical Chromid Candida diagnostic plates because storage temperature and time parameters were exceeded, preventing performance guarantees.

    Product
    PPM CLINICAL CRAPONNE CLINICAL CHROMID CANDIDA 20 PLATES, CATALOG 43631
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0866-2023·2023-01-11

    Biomerieux VIDAS Progesterone Tests Recalled for Storage Condition Failure

    Biomerieux is recalling VIDAS Progesterone 60 diagnostic tests (Batch 1009375960) nationwide due to storage temperature and time conditions being exceeded, preventing guaranteed product performance.

    Product
    VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS, CATALOG 30409-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0860-2023·2023-01-11

    ETEST Vancomycin Susceptibility Test Recalled Due to Storage Damage

    Biomerieux recalled ETEST vancomycin susceptibility tests after storage temperature and time excursions that may compromise product reliability and test accuracy.

    Product
    ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788
    Category
    Medical Device
    Distribution
    Distributed nationwide