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.

15976–16000 of 53092

  • HighNHTSA·22V702000·2022-09-19

    Tesla Model 3 window automatic reversal system may pinch occupants

    Tesla recalls 2017–2022 Model 3, 2020–2022 Model Y, and 2021–2022 Model S/X vehicles whose automatic window reversal system may fail to detect obstructions and pinch occupants. A free software update will fix the issue.

    Product
    TESLA — TESLA MODEL 3, MODEL Y, MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V699000·2022-09-19

    Collins School Bus Recall for Incorrect Emergency Exit Labels

    Collins Bus is recalling 2012-2020 school buses because emergency exit labels may be misplaced or too small, potentially delaying escape during an emergency.

    Product
    COLLINS — COLLINS DE, TL, TH, SL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V698000·2022-09-19

    Prevost Recalls X3-45 Commuter Motorcoaches Due to Incorrect Seat Belt Type

    Prevost is recalling 2021-2023 X3-45 Commuter motorcoaches because the driver's seat has a Type 1 seat belt instead of the required Type 2, which may not adequately protect the driver in a crash.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09162022-01·2022-09-16

    Tampa Bay Fisheries Chicken Entrees Recalled for Undeclared Egg Allergen

    USDA FSIS issued a public health alert for raw chicken entrees containing undeclared egg. Consumers with egg allergies should not consume these products.

    Product
    Tampa Bay Fisheries, Inc. — FSIS Issues Public Health Alert For Chicken Entree Products Due To Misbranding And An Undeclared Allergen
    Category
    Food
    Distribution
    7 states
  • HighNHTSA·22V696000·2022-09-16

    Winnebago Travato motorhomes recalled for unintended awning extension

    Winnebago is recalling certain 2019-2023 Travato motorhomes because the retractable awning may extend unintentionally during transit. An extended awning could become a distraction or road hazard, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V694000·2022-09-16

    Coachmen motorhomes recalled for improperly tightened LPG quick disconnect

    Forest River is recalling certain 2022-2023 Coachmen Leprechaun, Freelander, and Prism motorhomes due to an improperly tightened auxiliary LPG quick disconnect that could cause a gas leak and increase fire risk.

    Product
    COACHMEN — COACHMEN LEPRECHAUN, FREELANDER, PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V695000·2022-09-16

    Motorhome Retractable Awning Unintended Extension During Transit Recall

    Winnebago and Itasca motorhomes have a defective retractable awning that may extend unintentionally while driving. This can distract drivers or create a road hazard, potentially increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ERA, VIEW, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22222·2022-09-15

    Cervélo R5 and Caledonia-5 Bicycles Recalled for Fall Hazard

    Cervélo USA recalls about 1,800 Model Year 2022 R5 and Caledonia-5 bicycles and 182 ST31 LT replacement stems because handlebars can slip in the stem, causing loss of control and falls. One injury from a fall has been reported.

    Product
    Model Year 2022 Cervélo R5 and Caledonia-5 bicycles and Cervélo ST31 LT replacement stems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V691000·2022-09-15

    International commercial vehicles recalled for engine connecting rod failure

    Navistar is recalling certain 2018-2021 International HV, HX, LT, and RH vehicles because connecting rod wrist pins may crack, causing engine failure. This could lead to engine shutdown and increase the risk of a crash.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH, HX, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22772·2022-09-15

    Baby Trend Cityscape Travel Jogger Strollers Parking Brake Failure Recall

    Baby Trend is recalling about 310 Cityscape Travel Jogger Strollers (Model TJ75B12A) because the parking brake can fail, creating a fall and injury risk for children. No injuries have been reported.

    Product
    Cityscape Travel Jogger Strollers, Model TJ75B12A
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1711-2022·2022-09-14

    Piantedosi Seeded SPR Rolls recalled for potential bacterial contamination

    Piantedosi Baking Co. is recalling Seeded SPR Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected products were distributed across 15 states.

    Product
    Seeded SPR Roll 12-pack (033474501360)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1489-2022·2022-09-14

    Diphenhydramine HCl Oral Solution Recalled for Manufacturing Process Deviations

    Plastikon Healthcare LLC is recalling 349,100 cups of Diphenhydramine HCl Oral Solution due to manufacturing process control deviations. The product was distributed nationwide for institutional use only.

    Product
    Diphenhydramine HCl Oral Solution, 25 mg / 10 mL, 10 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6741-72
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1718-2022·2022-09-14

    Sunset Burger Roll 12-pack Recalled Due to Bacterial Contamination Risk

    Piantedosi Baking Co. is recalling Sunset Burger Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected lots were distributed across 15 states.

    Product
    Sunset Burger Roll 12-pack (033474504187)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1499-2022·2022-09-14

    Difluprednate Eye Drops Recalled for Defective Container Sterility Risk

    Cipla is recalling 117,844 bottles of Difluprednate eye drops nationwide due to defective containers where the protective cap can break, potentially exposing the dropper tip and compromising sterility.

    Product
    DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2022·2022-09-14

    ChemoLock Chemotherapy Port Connectors Recalled for Disconnection Risk

    ICU Medical recalls ChemoLock and ChemosafeLock port connectors used in chemotherapy delivery systems due to spring defects that may prevent proper connection or cause unintended disconnection, potentially delaying treatment or exposing patients to caustic substances.

    Product
    Product Description/Item: ChemoLock Vial Spike, 20mm/011-CL-80S; ChemoLock Bag Spike/CL-10; ChemoLock w/Mini Bag Spike/CL-17; 8 IN (20cm) APPX 1.0ml, EXT SET, MicroClave Clear, ChemoLock PORT, YCONN/CL3950; 31" (79 cm) Appx 3.4 ml, Admin Set w/20 Drop Integrated ChemoLock…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1494-2022·2022-09-14

    Children's Cough Medicine Recalled for Manufacturing Control Deficiency

    CORRECTDOSE Children's Cough & Chest Congestion DM is being recalled nationwide due to manufacturing process control deviations that did not meet required quality standards.

    Product
    CORRECTDOSE Children's COUGH & CHEST CONGESTION DM (Guaifenesin 100 mg / Dextromethorphan 5 mg per 5 mL) 2.04FL. OZ (60mL), packaged in 12-5 individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-321-05 UPC 8 60003 67146 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1712-2022·2022-09-14

    Clustered Potato Burger Rolls Recalled Due to Potential Bacterial Contamination

    Piantedosi Baking Co., Inc. is recalling Clustered Potato Burger Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects products distributed across 15 states.

    Product
    Clustered Potato Burger Roll 12-pack (033474502855)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1701-2022·2022-09-14

    Select Bakery Vanilla Creme Cake recalled for undeclared soy and food dyes

    Select Bakery Old Fashion Vanilla Creme Cake is being recalled due to undeclared soy and artificial food dyes (Yellow #5, Yellow #6, and Red #40). The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Old Fashion Vanilla Creme Cake Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10009 4
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-1496-2022·2022-09-14

    Sodium Chloride Ophthalmic Ointment Recalled for Turbidity and Sterility Concerns

    Akorn, Inc. is recalling Sodium Chloride Ophthalmic Ointment due to turbidity found during sterility testing. The FDA expanded the recall to additional lots sharing potential root cause.

    Product
    Sodium Chloride Ophthalmic Ointment USP, 5%, Sterile, Net Wt 3.5 g (1/8 oz) tube, Mfg by: Akorn, Inc., Lake Forest , IL 600405, NDC 17478-622-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1679-2022·2022-09-14

    Abbott Alinity m SARS-CoV-2 Control Kit Recalled for Failed Internal Control

    Abbott is recalling 579 kits of its Alinity m SARS-CoV-2 CTRL control kit after reports of failed internal control errors preventing verification of test accuracy.

    Product
    Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In Vitro Diagnostic Use.
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Food)·F-1704-2022·2022-09-14

    Select Bakery Walnut Brownies Recalled for Undeclared Soy and Red #40

    Select Bakery Walnut Brownies are being recalled due to undeclared soy and Red #40. The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Walnut Brownie Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10006 3
    Category
    Food
    Distribution
    3 states