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Mckesson Information Solutions LLC

Mckesson Information Solutions LLC Recalls

All product recalls associated with Mckesson Information Solutions LLC.

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

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 12721–12740 of 17593 recalls

McKesson Cardiology Hemo (Mckesson) – Hemoglobin Calculation Error (2014)

Software Error: The McKesson Cardiology Hemo calculation section incorrectly converts the Hemoglobin value before it is utilized in the applicable formula calculations.

Class IIModerate

FDAAug 27, 2014Nationwide• Mckesson Information Solutions LLC

Notebook Power Cords (HP) – fire hazard (2014)

Fire/Burn Risk

This recall involves Hewlett-Packard's LS-15 AC power cord. The power cords were distributed with HP and Compaq notebook and mini notebook computers and with AC adapter-powered accessories such as docking stations. The power cords are black in color and have an "LS-15" molded mark on the AC adapter end of the power cord.

CPSCAug 26, 2014Nationwide• Hewlett-Packard Company (HP), of Palo Alto, Calif.

Coulter DxH Diluent (Beckman) – Platelet Count Elevation (2014)

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Beckman Coulter is recalling Coulter DxH Diluent because it may be associated with elevated platelet (PLT) background counts between 3-7 x 10(3) cells/uL. This will result in failed Daily Checks on the UniCel DxH 800 and DxH 600 Coulter Cellular Analysis Systems.

Class IIModerate

FDAAug 25, 2014Nationwide• Beckman Coulter Inc.

Activia Blueberry Yogurt (Dannon) - Potential Ingredient Issue (2014)

The recalled product includes an ingredient (condensed skim milk) that the supplier Dairy Farmers of America has advised may have been produced from raw milk that has tested positive for the presence of sulfamethazine antibiotic.

Class IIILow

FDAAug 25, 2014FL, GA, IL +7 more• The Dannon Company, Inc - Discovery & Innovation Center

Liquid Vitamin C (Hi-Tech Pharmacal) - Low Active Ingredient (2014)

The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.

Class IIILow

FDAAug 25, 2014CA, FL, ID +10 more• Hi-Tech Pharmacal Co., Inc.

Mixed Greens (McCall Farms) - Swollen Cans Illness (2014)

Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products.

Class IIILow

FDAAug 22, 2014GA, MD, NJ +6 more• Mccall Farms Inc

Turnip Greens (McCall Farms) - Swollen Cans Illness (2014)

Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products.

Class IIILow

FDAAug 22, 2014GA, MD, NJ +6 more• Mccall Farms Inc

UniCel Immunoassay System (Beckman) – Sample Probe Issue (2014)

Beckman Coulter is recalling the Sample Probe Cable because nonconforming sample probe cables may been installed on newly manufactured and/or recently serviced UniCel DxI 600 and 800 Access Immunoassay Systems, UniCel DxC 660i, 680i, and 860i, and UniCel DxC 880i Synchron Access Clinical Systems instruments. Use of a nonconforming sample probe cable can casuse a delay in reporting results, but wi

Class IIModerate

FDAAug 21, 2014Nationwide• Beckman Coulter Inc.

TEGRIS System (Maquet) – Movement Control Error (2014)

The wrong movement results on the MAGNUS OR table. The button commands on the TEGRIS touchscreen for Lower Leg Up and Upper Leg Down are switched in the software for the integration with the MAGNUS operating table system.

Class IIModerate

FDAAug 21, 2014Nationwide• Maquet Medical Systems USA

MR Systems (Philips) – Image Order Reversal (2014)

When a fused series of a sagittal, coronal or radial multi station scan is generated in MobiView, the resultant image order is reversed. This occurs with software release R5.1.7/R5.1.8.

Class IIModerate

FDAAug 21, 2014Nationwide• Philips Medical Systems, Inc.

Hercules Stabilizing Arm (Terumo) – Pin Failure Risk (2014)

Terumo Cardiovascular Systems (Terumo CVS) is recalling certain lots of Hercules TM 360 Universal Stabilizing Arms because the two pins that hold the sleeve attached to the distal end of the device may come loose, causing the pins and sleeve to separate from the device. While the arm can still function without the pins and sleeve in place, there is potential for the loose components to fall into the surgical site.

Class IIModerate

FDAAug 20, 2014Nationwide• Terumo Cardiovascular Systems Corporation

Primary IV Set (ICU Medical) – Flow Rate Problem (2014)

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

Ellipse Defibrillators (St Jude) – High Voltage Therapy Risk (2014)

An anomaly may result in delayed, partial, or no delivery of high voltage therapy. Internal damage to the high voltage capacitors, which may result in extended charge time, occurring during capacitor maintenance or charging for high voltage therapy. It may present as a vibratory patient notification and upon interrogation, a programmer or Merlin.net alert.

Class IIModerate

FDAAug 19, 2014Nationwide• St Jude Medical Cardiac Rhythm Management Division

STAT 2 Flow Controller (ICU Medical) – Flow Rate Problem (2014)

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

Primary IV Set (ICU Medical) – Flow Rate Problem (2014)

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

Patient Support (Philips) – Footplate Fall Risk (2014)

The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.

Class IIModerate

FDAAug 19, 2014AZ, CT, FL +9 more• Philips Medical Systems, Inc.

Mason Convertible Cribs (Bexco) - Fall Hazard (2014)

This recall includes Franklin & Ben Mason style 4-in-1 style cribs model number 5601 that were manufactured from January 2012 through August 2012. The model number and the date of manufacture are printed on a label on the inside of a side panel of the crib. Listed on the label as a "serial number," the following purchase order numbers are included in the recall: H004522, H004546, H004548 or H004777. The cribs have solid wood sideboards and wood rails on the front and back of the crib in varying heights and can convert to a daybed, toddler bed or full-sized bed. There is a storage drawer at the base of the crib with two metal knobs. The recalled cribs were sold in weathered gray and rustic brown, and measure 57 inches long by 33 inches wide by 51 inches high.

CPSCAug 19, 2014Nationwide• Bexco Enterprises Inc., of Montebello, Calif.

Patient Support (Philips) – Footplate Fall Risk (2014)

The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.

Class IIModerate

FDAAug 19, 2014AZ, CT, FL +9 more• Philips Medical Systems, Inc.

STAT 2 Flow Controller (ICU Medical) – Flow Rate Problem (2014)

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

Echelon Oval MRI (Hitachi) – Gradient Coil Burn Risk (2014)

Fire/Burn Risk

The Gradient Coil was found to have a failure mode that allowed it to overheat and become a burn hazard.

Class IIModerate

FDAAug 18, 2014Nationwide• Hitachi Medical Systems America Inc