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Bruder Healthcare Company, LLC

Bruder Healthcare Company, LLC Recalls

All product recalls associated with Bruder Healthcare Company, LLC.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 2821–2840 of 25002 recalls

Thermalon Sinus Compress French (Bruder) – Moisture Exposure Risk (2024)

Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

Moderate

FDAFeb 21, 2024Nationwide• Bruder Healthcare Company, LLC

Thermalon Eye Compress (Bruder) – Moisture Exposure Risk (2024)

Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

Moderate

FDAFeb 21, 2024Nationwide• Bruder Healthcare Company, LLC

Thermalon Neck Wrap (Bruder) – Moisture Exposure Risk (2024)

Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

Moderate

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FDA

Feb 21, 2024

Nationwide

• Bruder Healthcare Company, LLC

Thermalon Back Wrap (Bruder) – Moisture Exposure Risk (2024)

Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

Moderate

FDAFeb 21, 2024Nationwide• Bruder Healthcare Company, LLC

HydroFlock Collection Device (Puritan) – Mislabeled Product (2024)

It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in all packages.

High

FDAFeb 21, 2024Nationwide• Puritan Medical Products Company, Llc

MediBeads Neck Wrap (Bruder Healthcare) – Moisture Risk (2024)

Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.

Moderate

FDAFeb 21, 2024Nationwide• Bruder Healthcare Company, LLC

3M Tube Securement Device (3M) – Manufacturing Defect (2024)

Manufacturing nonconformities are in some lots of the Tube Securement Device, such as the top film layer may be partially or completely missing and some devices may exhibit the appearance of an incorrect shape due to excess material not being removed from the product liner.

Moderate

FDAFeb 20, 2024Nationwide• 3M Company Health Care Business 3m Center

Cardiovascular Procedure Kits (Terumo) – Pressure Valve Issue (2024)

Pressure relief valve included in certain lots of cardiovascular procedure kits was reportedly opening at approximately 200-300mmHg versus 400mmHg, potential myocardial tissue damage potentially requiring surgical or medical/pharmacological intervention

High

FDAFeb 20, 2024Nationwide• Terumo Cardiovascular Systems Corporation

Clindamycin Phosphate Solution (Contract Pharmaceuticals) – container defect (2024)

Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.

Class IIILow

FDAFeb 20, 2024Nationwide• Contract Pharmaceuticals Limited Canada

Clindamycin Phosphate Solution (Contract Pharmaceuticals) – container defect (2024)

Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.

Class IIILow

FDAFeb 20, 2024Nationwide• Contract Pharmaceuticals Limited Canada

Raw Cheddar Cheese (Raw Farm) – E. Coli Risk (2024)

E. coli

Potential contamination with E. coli O157:H7

Class IHigh

FDAFeb 16, 2024AZ, CA, CO +2 more• Raw Farm LLC

Raw Cheddar Cheese (Raw Farm) – E. Coli Contamination (2024)

E. coli

Potential contamination with E. coli O157:H7

Class IHigh

FDAFeb 16, 2024AZ, CA, CO +2 more• Raw Farm LLC

Raw Cheddar Cheese (Raw Farm) – E. Coli Risk (2024)

E. coli

Potential contamination with E. coli O157:H7

Class IHigh

FDAFeb 16, 2024AZ, CA, CO +2 more• Raw Farm LLC

Rad-G Pulse Oximeter (Masimo) – Power Monitoring Risk (2024)

Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.

Moderate

FDAFeb 15, 2024Nationwide• Masimo Corporation

HotDog Return Electrode (Augustine) – Electrode Contact Issue (2024)

Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .

Low

FDAFeb 15, 2024AL, NV, TX• Augustine Temperature Management, LLC

DIVA LCD Display (Philips) – Touch Input Malfunction (2024)

If the DIVA touch display generates touch inputs without user interaction, due to possibility of the erroneous acknowledgement of a patient alarm, there is a potential for a delay in the detection of a change in a patient condition which prompted the alarm to generate. Although unlikely, this could potentially result in a patient harm.

Moderate

FDAFeb 15, 2024Nationwide• Philips North America Llc