The Recall Desk

Archive

August 2025 recalls

523 recalls were announced in August 2025.

What the numbers show

Critical
39
Severe
106
High
239
Moderate
138
Low
1

Of the 523 recalls this month scored against our rubric, 7% are Critical, 20% are Severe.

Which agencies issued them

501–523 of 523

  • ModerateFDA (Devices)·Z-2197-2025·2025-08-06

    IontoPatch 80 nonwoven pads do not absorb the saline solution

    IontoPatch 80 On-the-Go Patch Therapy is being recalled because the nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with it. 63,936 units affected.

    Product
    IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0339-2025·2025-08-06

    Suspiros cajeta cake contains goat milk labeled only as milk

    Suspiros Cajeta Cake is being recalled because it contains goat milk, which was labeled simply as "milk". 268 units are affected.

    Product
    Suspiros Cajeta Cake. 15 P: 20 servings (2000 gr), 4P: 4.8 servings (480gr). UPC= 15P: 1338, 4P: 6965. Type of packaging: Plastic dome and plate (15P and 4P). Firm name: NOVACAB SAPI de CV. Address listed on label: El paso, TX 79901, USA.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·H-0342-2025·2025-08-06

    Suspiros choconut cake contains goat milk labeled only as milk

    Suspiros Choconut Cake is being recalled because it contains goat milk, which was labeled simply as "milk". 124 units are affected.

    Product
    Suspiros Choconut Cake. 15 P: 36.7 servings (2018 gr), 4P: 9.9 servings (544 gr). UPC= 15P: 1300, 4P: 698. Type of packaging: Plastic dome and plate (15P and 4P). Firm name: NOVACAB SAPI de CV. Address listed on label: El paso, TX 79901, USA.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2190-2025·2025-08-06

    BostonSight scleral lenses made with sagittal height or haptic errors

    BostonSight SCLERAL Lenses are being recalled because select orders were manufactured with errors impacting sagittal height, haptics, or both. 441 units are affected.

    Product
    BostonSight SCLERAL Lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0346-2025·2025-08-06

    Cajeta cupcakes contain goat milk labeled only as milk

    Cajeta cupcakes and other cake products are being recalled because they contain goat milk, which was labeled simply as "milk". 24 units are affected.

    Product
    Cajeta cupcakes (Box). Vanilla cake decorated with suspiros cream and dulce de leche-milk caramel filling. Blister plastic tray with lid (Box). Box: 6 servings (438 gr). Box: SKU89
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2196-2025·2025-08-06

    IontoPatch STAT nonwoven pads do not absorb the saline solution

    IontoPatch STAT On-the-Go Patch Therapy is being recalled because the nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with it. 80,928 units affected.

    Product
    IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2172-2025·2025-08-06

    Sterilizable Drill Stop Kits were shipped containing incorrect components

    The Drill Stop Kit, a version of the Mini Sterilizable Tray used to store, sterilize and verify drill stop length, is being recalled because it contains incorrect components. 45 kits affected.

    Product
    The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit includes the Release Bracket, which is used for mounting and removing Drill…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0338-2025·2025-08-06

    Suspiros tres leches cajeta cake contains goat milk labeled as milk

    Suspiros Tres Leches Cajeta Cake is being recalled because it contains goat milk, which was labeled simply as "milk". 1,249 units are affected.

    Product
    Suspiros Tres Leches Cajeta Cake. 15 P: 25 servings (2500 gr), 4P: 7 servings (700gr), Pocket: 3.7 servings (370gr). UPC= 15P: 1335, 4P: 6982, POCKET: 35256. Type of packaging: Plastic dome and plate (15P and 4P) and Blister plastic tray with lid (in Pocket presentation). Firm…
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2191-2025·2025-08-06

    BostonSight PROSE lenses made with sagittal height or haptic errors

    BostonSight PROSE Lenses are being recalled because select orders were manufactured with errors impacting sagittal height, haptics, or both. 38 units are affected.

    Product
    BostonSight PROSE Lens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0542-2025·2025-08-06

    Amlodipine and benazepril capsules released with the wrong expiry date

    Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg are being recalled because they were released with the wrong expiry date, printed as February 2027 instead of January 2027. 7,668 bottles affected.

    Product
    AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE (AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0543-2025·2025-08-06

    Timolol eye drop caps can lodge a spike in the nozzle

    Timolol Maleate Ophthalmic Solution USP 0.5% is being recalled because of a defective container: the spike of the cap becomes lodged in the nozzle of the bottle. 154,176 bottles affected.

    Product
    TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2192-2025·2025-08-06

    Phasor neurosurgical drills may have a reverse battery orientation

    The Phasor Drill, used in neurosurgical procedures, is being recalled because it may have a reverse battery orientation, which may increase surgical time. 1,064 units are affected.

    Product
    Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-2219-2025·2025-08-06

    ASPIRE Cristalle mammography systems shipped with unapproved slabbing software enabled

    ASPIRE Cristalle Mammography Systems with the Digital Breast Tomosynthesis option are being recalled because devices had an unapproved slabbing software function enabled for use. 293 units affected.

    Product
    ASPRIRE Cristalle Mammography System (cleared under K212873) installed with the ASPIRE Cristalle Digital Breast Tomosynthesis (DBT) Option (approved under P160031).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0345-2025·2025-08-06

    Suspiros German cake contains goat milk labeled only as milk

    Suspiros German Cake is being recalled because it contains goat milk, which was labeled simply as "milk". 93 units are affected.

    Product
    Suspiros German Cake. 15 P: 37.5 servings (2062 gr), 4P: 10 servings (550gr). UPC= 15 P: 1342, 4P: 6971. Type of packaging: Plastic dome and plate (15P and 4P). Firm name: NOVACAB SAPI de CV. Address listed on label: El paso, TX 79901, USA.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0547-2025·2025-08-06

    Sucralfate tablets recalled because bankruptcy left the quality program unmonitored

    Sucralfate Tablets USP 1 gram from Nostrum Laboratories are being recalled across all lots within expiry because the firm cannot monitor its quality program after filing for Chapter 11. 60,608 bottles affected.

    Product
    Sucralfate Tablets, USP 1 gram, packaged in a) 100-count bottles NDC 29033-0003-01, and b) 500-count bottles, NDC 29033-0003-05), Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0381-2025·2025-08-06

    Pure Monk Fruit Sweetener bottles actually contain mislabeled stevia powder

    Pure Monk Fruit Sweetener, 0.71 oz, is being recalled because the product is stevia powder but the bottle was mislabeled as Pure Monk Fruit Sweetener. 78 bottles are affected.

    Product
    Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap. Ingredient: Monk Fruit (Luo Han Guo) Extract. Monk Fruit is so much sweeter than sugar, a pinch is all you need. Suggested Use: Add to sweeten your food or…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0341-2025·2025-08-06

    Suspiros four leches cake contains goat milk labeled only as milk

    Suspiros 4 Leches Cake is being recalled because it contains goat milk, which was labeled simply as "milk". 612 units are affected.

    Product
    Suspiros 4 Leches Cake. 15 P: 26 servings (2600 gr), 4P: 7 servings (700 gr), Pocket: 4.1 servings (410gr). UPC=15P: 1343, 4P: 6969, POCKET: 7904. Type of packaging: Plastic dome and plate (15P and 4P) and Blister plastic tray with lid (in Pocket presentation). Firm name…
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·25V501000·2025-08-05

    2024–2026 International LT and 2025 RH Trucks Service Brake Defect

    International Motors is recalling certain 2024–2026 LT and 2025 RH trucks because the Hill Start Assist exhaust port may clog, preventing brake release and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E049000·2025-08-05

    Holley Recalls 140 GPH Electric Fuel Pumps Due to Methanol Incompatibility

    Holley Performance Products is recalling 140 GPH BLACK electric fuel pumps because they may not be compatible with methanol fuel, which can cause leaks and fire risks.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V499000·2025-08-04

    2024-2025 Winnebago Ekko RV Tire Valve Extension Defect Recall

    Winnebago is recalling certain 2024-2025 Ekko recreational vehicles due to damaged tire valve extensions that can cause air loss in the inner tire and overload the outer tire, creating a crash risk. Dealers will replace the extensions free of charge.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E048000·2025-08-01

    Bendix Recalls Knorr-Bresme Brake Chambers for Fire Risk

    Bendix is recalling specific Knorr-Bresme brake chambers for buses due to improper manufacturing that can cause air leaks and increase fire risk.

    Product
    PARKING BRAKE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

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