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Ascent Consumer Products Inc.

Ascent Consumer Products Inc. Recalls

All product recalls associated with Ascent Consumer Products Inc..

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 881–900 of 17592 recalls

SinuCleanse Saline Packets (Ascent) – Bacterial Contamination (2025)

Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus

Class IHigh

FDAJan 28, 2025Nationwide• Ascent Consumer Products Inc.

SinuCleanse Soft Tip Bottle (Ascent) – Bacterial Contamination (2025)

Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus

Class IHigh

FDAJan 28, 2025Nationwide• Ascent Consumer Products Inc.

Dexcom G6 Monitoring System (Dexcom) – alert failure (2025)

Under very rare situations, the Dexcom G6 touchscreen receiver may not provide high or low glucose alarms/alerts as designed, which can result in two different conditions. First, if a receiver operating system .net error occurs when an alarm/alert should be triggered, the initial alarm/alert will not be delivered until a subsequent alarm/alert is triggered. At that time, the initial alarm/alert is delivered, but not the second one. Alarm/alerts will continue to be delayed and be one alarm/alert behind, causing delayed alarm/alerts until the receiver is reset. This condition could result in the missed detection of a hyperglycemic or hypoglycemic event. Second, a single EGV reading may be delayed for 5 minutes after the initial .net operating system error. If the user receives a single EGV reading delayed by 5 minutes, the delay is not expected to cause user harm.

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Moderate

FDAJan 27, 2025Nationwide• Dexcom, Inc.

Prelude IDEAL Sheath Introducer (Merit) – incorrect dilator (2025)

Hydrophilic Sheath Introducer labeled for 4F dilators may instead incorrectly contain 5F dilators. Incorrect dilator use may result in procedure delay.

Low

FDAJan 27, 2025Nationwide• Merit Medical Systems, Inc.

Dark Chocolate Pretzels (Woodstock Farms) – Undeclared Milk (2025)

Undeclared Allergen

Undeclared Allergen - Milk

Class IHigh

FDAJan 27, 2025NY• United Natural Trading Inc. dba Woodstock Farms

Coachmen Catalina Trailer (Coachmen) – incorrect placard (2025)

Forest River, Inc. (Forest River) is recalling certain 2025 Coachmen Catalina travel trailers. The Federal Placard label lists an incorrect vehicle dry weight.

High

NHTSAJan 24, 2025Nationwide• COACHMEN

Timolol Maleate Eye Solution (FDC) – Defective Container (2025)

Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.

Class IIModerate

FDAJan 23, 2025IN, NJ• FDC Limited

Lorazepam Tablets 1mg (Major) – Potency Concern (2025)

Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.

Class IIModerate

FDAJan 21, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Lorazepam Tablets 0.5mg (Major) – Potency Concern (2025)

Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.

Class IIModerate

FDAJan 21, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Lorazepam Tablets 2mg (Major) – Potency Concern (2025)

Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.

Class IIModerate

FDAJan 21, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Cummins L9 Engine (Cummins) – fuel hose separation (2025)

Fire/Burn Risk

Cummins Inc. (Cummins) is recalling certain L9 diesel engines, part number D563027BX03. The remote fuel filter hoses may separate from the fitting, causing a fuel leak and an engine stall.

High

NHTSAJan 17, 2025Nationwide• CUMMINS

Badger Sunscreen SPF 50 (Badger) – Labeling Omission (2025)

Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.

Class IIILow

FDAJan 17, 2025Nationwide• The W.S. Badger Company, Inc.

Quantum Perfusion Blood Pump (Spectrum) – fluid leakage (2025)

Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.

Moderate

FDAJan 16, 2025Nationwide• Spectrum Medical Inc

RayStation Planning System (RaySearch) – density uncertainty (2025)

Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a HU-to-mass density CT calibration curve used in RayStation version 4.5 to 2024B including some service packs.

Moderate

FDAJan 16, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Ranger XD 1500 ROVs (Polaris) – Vehicle Safety Issue (2025)

This recall involves certain VINs of Polaris Model Year 2024-2025 RANGER XD 1500 and RANGER CREW XD 1500 ROVs. The recalled ROVs were sold in camouflage, red, silver and titanium colors. The vehicles were sold in three- and six-seat configurations and have "POLARIS" stamped on the front grille. The VIN is printed on a portion of the left rear frame (on the driver's side of the vehicle) under the cargo box. In addition, this recall involves doors purchased as an accessory with part numbers 2212292, 2212291, 2638498, 2638499, 2638500, 2638501, 2889075 or 2889076. All accessory doors purchased for Polaris Model Year 2024-2025 RANGER XD 1500 and RANGER CREW XD 1500 ROVs prior to November 11, 2024 are affected by this recall.

High

CPSCJan 16, 2025Nationwide• Polaris Industries Inc., of Medina, Minnesota

Venlafaxine Tablets (Appco Pharma) – Missing Tablet ID (2025)

Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet

Class IIILow

FDAJan 16, 2025Nationwide• Appco Pharma LLC

Single Use Guide Sheath Kit (Olympus) – radiopaque tip risk (2025)

Potential for the radiopaque tip of the guide sheath component to disassociate and fall off into the patient.

High

FDAJan 15, 2025Nationwide• Olympus Corporation of the Americas

Monkfish Liver (Mutual Trading) – Undeclared Milk (2025)

Undeclared Allergen

Imported Monkfish Liver undeclared allergen (Milk)

Class IHigh

FDAJan 15, 2025CT, FL, GA +5 more• Mutual Trading Company Inc.

Infinity Central Station (Draeger) – Speaker Malfunction (2025)

Edifier speakers (shipped in or after April 2023) may not annunciate when configured in analog mode which can lead to delayed treatment to the patient.

High

FDAJan 14, 2025Nationwide• Draeger Medical Systems, Inc.

Allura CV20 (Philips) – Safety Issue (2025)

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

High

FDAJan 13, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands