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MEDLINE INDUSTRIES, LP Northfield

MEDLINE INDUSTRIES, LP Northfield Recalls

All product recalls associated with MEDLINE INDUSTRIES, LP Northfield.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 4201–4220 of 37665 recalls

Centurion Dental Rolls (MEDLINE) – Weak Seal Risk (2024)

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Moderate

FDAFeb 23, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Centurion Skin Hook (MEDLINE) – Weak Seal Risk (2024)

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Moderate

FDAFeb 23, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Raiz de Tejocote Supplements (Backstage Center) - toxic ingredient (2024)

The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

Class I

1...209 210211212 213...1884

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High

FDAFeb 23, 2024Nationwide• Backstage Center DBA CTC Seller

Centurion Ear Speculum Set (MEDLINE) – Weak Seal Risk (2024)

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Moderate

FDAFeb 23, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Centurion Kelly Hemostat (MEDLINE) – Weak Seal Risk (2024)

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Moderate

FDAFeb 23, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

MATRYX Snowmobiles (Polaris) – Injury Risk (2024)

This recall involves certain Polaris Model Year 2022-2024 MATRYX Voyageur, Indy, Switchback, RMK, and SKS snowmobiles. The recalled snowmobiles were sold in black and custom color combinations and equipped with PATRIOT 650 and 850 engines. The recall also includes primary (drive) clutches sold as service parts with part numbers 1323613 (e-start) and 1323614 (manual start). "POLARIS" is stamped on the front side panel of the vehicles. The VIN and model number are located on the right side of the vehicle's frame. The following models are being recalled: Recalled Model Description Recalled Snowmobiles Model Description Model Year 2022 650 MATRYX VOYAGEUR 146 Model Year 2022 650 MATRYX INDY Model Year 2022 850 MATRYX INDY Model Year 2022 650 MATRYX SWITCHBACK Model Year 2022 850 MATRYX SWITCHBACK Model Year 2022 650 MATRYX RMK Model Year 2022 850 MATRYX RMK Model Year 2023 650 MATRYX INDY Model Year 2023 850 MATRYX INDY Model Year 2023 650 MATRYX SWITCHBACK Model Year 2023 850 MATRYX SWITCHBACK Model Year 2023 650 MATRYX VOYAGEUR 146 Model Year 2023 650 MATRYX SKS 146 Model Year 2023 650 MATRYX RMK Model Year 2023 850 MATRYX RMK Model Year 2024 850 MATRYX RMK

High

CPSCFeb 22, 2024Nationwide• Polaris Industries Inc., of Medina, Minnesota

Surgical Tools Marketing Brochure (Baxter) – Incorrect Information (2024)

The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).

Moderate

FDAFeb 22, 2024Nationwide• Baxter Healthcare Corporation

RELAY PRO Stent-Graft (Bolton Medical) – Incorrect Size (2024)

The stent-graft inside the delivery system was the incorrect size.

High

FDAFeb 22, 2024Nationwide• Bolton Medical Inc.

Organic Carrot Juice (Barsotti) – Under Processed (2024)

Product was determined to be under processed.

Class IIModerate

FDAFeb 22, 2024AZ, CA, CT +7 more• Barsotti Juice Company, Inc.

Thermalon Stye 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

MediBeads King Pad (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 Sinus 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 Heating Pad (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 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

ARCHITECT Myoglobin Reagent Kit (Abbott) – Calibration Failure (2024)

The reason for the recall is the failure of calibration and quality controls due to a manufacturing issue of microparticles not meeting labeled claim. This may lead to incorrect myoglobin results and delayed diagnosis of myocardial infarction.

High

FDAFeb 21, 2024Nationwide• Abbott Laboratories

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

FDAFeb 21, 2024Nationwide• 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