Thermalon Neck Wrap recalled due to potential mold and mildew growth
Bruder Healthcare Company is recalling Thermalon Neck Wrap (Item Number 24322) from certain lots due to potential mold and mildew growth from excessive moisture exposure. Consumers should discontinue use and contact the manufacturer.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II device recall with no reported illnesses or injuries and a theoretical hazard (potential mold and mildew growth). Per the rubric, low-risk contamination with no reported incidents qualifies as Moderate severity.
Plain-English summary
Bruder Healthcare Company is recalling the Thermalon Neck Wrap, Item Number 24322, from certain lots. The moist heat wrap may have been exposed to excessive moisture during distribution or storage, which could result in mold and/or mildew growth.
Approximately 471 units are affected. The recall involves lot numbers M053560 and M053140, which can be identified using UPC 041533243229. The product was distributed worldwide, including throughout the United States and Canada.
Consumers who have an affected Thermalon Neck Wrap should stop using the product and contact Bruder Healthcare Company for further instructions.
The recalled product
- Product
- Thermalon Neck Wrap, Item Number 24322
- Manufacturer
- Bruder Healthcare Company, LLC
- Affected units
- 471
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- UPC 041533243229
- Lot Numbers: M053560
- M053140
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 9 recalled by Bruder Healthcare Company, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 9 products in this recall →Related recalls
Same manufacturer · Bruder Healthcare Company, LLC
See all →- ModerateThermalon Heating Pads Recalled for Potential Mold and Mildew Growth
FDA (Devices) · 2024-04-03
- HighThermalon Eye Compress Recalled Due to Potential Mold and Mildew Growth
FDA (Devices) · 2024-04-03
- HighThermalon Sinus Compress Recalled for Potential Mold and Mildew
FDA (Devices) · 2024-04-03
- HighThermalon Sinus Compress Recalled for Potential Mold and Mildew Growth
FDA (Devices) · 2024-04-03
- HighThermalon Back Wrap Recalled for Potential Mold and Mildew Growth
FDA (Devices) · 2024-04-03
Same hazard · mold
See all →- CriticalUn-eviscerated fish recalled for botulism risk, mold and insect larvae
FDA (Food) · 2025-10-22
- HighHostess Ding Dongs recalled over mold traced to malfunctioning cooler
FDA (Food) · 2025-09-03
- HighGrains of Paradise spice recalled for potential mold contamination
FDA (Food) · 2024-12-04
- HighLunds & Byerlys Lone Star Dip Recalled for Potential Mold Contamination
FDA (Food) · 2024-10-23
- HighMontreal Fudge Chocolate Fudge with Nuts Recalled for Mold Contamination
FDA (Food) · 2024-10-02
Similar recalls
- CriticalTeleflex Recalls MAQUET SERVO Humidifiers Due to Cracked Flex Tubes
FDA (Devices) · 2015-02-18
- HighEmson Recalls UComfy Neck and Shoulder Heat Wraps Due to Burn Hazard
CPSC · 2016-07-27
- HighTerumo Medical Recalls 23G Needles Due to Potential Sterility Compromise
FDA (Devices) · 2019-07-31
- HighTeleflex Recalls RUSCH TruLite Disposable Laryngoscope Handles
FDA (Devices) · 2014-08-06
- HighTeleflex Servo Humidifier 163 Recalled Due to Connector Cracks
FDA (Devices) · 2016-08-17
- HighThermaCare HeatWraps Recalled for Potential Skin Burn Risk
FDA (Devices) · 2019-06-05