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Biocare Medical, LLC

Biocare Medical, LLC Recalls

All product recalls associated with Biocare Medical, LLC.

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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 1161–1180 of 17592 recalls

intelliPATH HRP Detection Kit (Biocare) – Weak Staining (2024)

Kits containing the DAB chromogen buffer, intended for use in either manual or automated Immunohistochemistry (IHC) staining protocols, may produce weak to no staining, which may lead to test failure requiring the test to be repeated.

Moderate

FDASep 25, 2024Nationwide• Biocare Medical, LLC

Norepinephrine Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Norepinephrine Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

1...57 585960 61...880

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FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Phenylephrine HCl Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Epinephrine Sodium Chloride (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Phenylephrine HCl Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Vancomycin HCl Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Phenylephrine HCl Injection (Fresenius Kabi) – Manufacturing Violations (2024)

CGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Phenylephrine HCl Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Oxytocin Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Thiamine HCl Injection (Fresenius Kabi) – Manufacturing Violations (2024)

cGMP violations

Class IIModerate

FDASep 25, 2024Nationwide• Fresenius Kabi Compounding, LLC

Cushman Hauler Pro LSV (Cushman) – Brake Linkage (2024)

Textron Specialized Vehicles (Textron) is recalling certain 2024-2025 E-Z-GO Liberty LSV, CUSHMAN Tour LSV and CUSHMAN Hauler Pro vehicles. The brake linkage rod may bend under applied force, impairing application of the brakes.

High

NHTSASep 24, 2024Nationwide• CUSHMAN

Quest Spectrum 3 System (Olympus) – EMC Compliance (2024)

Does not meet the requirements for electromagnetic compatibility (EMC) of the standard IEC 60601-1-2. Electromagnetic interference occurring during a procedure may cause the device to malfunction requiring the replacement of the device. This could potentially result in a prolonged procedure and/or require additional medical intervention

Moderate

FDASep 24, 2024OH• Olympus Corporation of the Americas

Grabeez Big Cheese Snack Mix (Tropical Nut) – Undeclared Nuts (2024)

Undeclared Allergen

Undeclared Almonds & Cashews. The firm was notified by their customers that the product contains a trail mix instead of the cheese mix. The trail mix contains almonds and cashews that are not listed in the ingredient statement.

Class IIModerate

FDASep 24, 2024FL, GA, IL +9 more• Tropical Nut & Fruit Company

Percept RC Neurostimulator (Medtronic) – Programming Compatibility (2024)

A limited number of Percept RC Implantable Neurostimulators (INS), Model B35300 will not be able to communicate with the A610 DBS Clinician Programmer Application upon use and an "Invalid Device" message will appear.

Low

FDASep 24, 2024Nationwide• Medtronic Neuromodulation

Cummins X15 Engine (Cummins) – Fuel System Issue (2024)

Cummins, Inc. (Cummins) is recalling certain X15 diesel engines with part number D103019BX03, Cummins X15 re-manufactured engines with part number DR7989-RX, Cummins X15 fuel pump barrel service kits with part number 631058000, 6310580PX, X15 fuel pump service assemblies, with part numbers 559463000, 559462500, 5594630PX, 5594625PX, and X15 overhaul kits, with part numbers 632445200RX and 632445500RX. The fuel pump barrels may fracture and cause a fuel leak, which can result in an engine stall.

High

NHTSASep 23, 2024Nationwide• CUMMINS

Sour Charlie Bread (Salt City Baking) – Undeclared Wheat (2024)

Undeclared Gluten

Undeclared Wheat flour. Product contains wheat flour but product was sold without the Ingredients Statement.

Class IIModerate

FDASep 23, 2024IN, UT• Salt City Baking Company, LLC

Cabinet Heaters (Caframo) – Electrocution Risk (2024)

Laceration Risk

This recall involves model 9421 Cabinet Heaters, primarily intended for keeping cabinets and parking ticket dispensers warm. The cabinet heater has a black painted steel enclosure and measures 5-3/4 inches wide by 9 inches long by 3-1/3 inches high. A serial plate, an on/off switch, and a label with "Model 9421" are located on the top of the heater, near the power cord.

High

CPSCSep 19, 2024Nationwide• Caframo Limited, of Canada

Polaris Ranger XD 1500 ROVs (Polaris) – Safety Issue (2024)

Fire/Burn Risk

This recall involves certain VINs of Polaris Model Year 2024 RANGER XD 1500 and RANGER CREW XD 1500 ROVs. The recalled ROVs were sold in camouflage, red and silver 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 4,500 and 6,000 lb. winches purchased as an accessory (part numbers 2889275 or 2889276).

High

CPSCSep 19, 2024Nationwide• Polaris Industries Inc., of Medina, Minnesota

AD-TECH Spencer Probe Depth Electrode (Ad-Tech) – Labeling Error (2024)

Ad-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly placed instead of the MR Unsafe symbol. The A style contacts were not cleared for MR Conditional use. Our records indicate you have received one or more of the affected lots listed above.

Moderate

FDASep 19, 2024Nationwide• Ad-Tech Medical Instrument Corporation