Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Mckesson Medical-Surgical Inc. Corporate Office

Mckesson Medical-Surgical Inc. Corporate Office Recalls

All product recalls associated with Mckesson Medical-Surgical Inc. Corporate Office.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

731

Class I (Serious)

175

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 981–1000 of 11123 recalls

Proparacaine Ophthalmic Solution (Mckesson) – Temperature Abuse (2024)

Temperature abuse: Products exposed to improper temperature above drug label specifications.

Class IIModerate

FDASep 11, 2024IN, MD, VA• Mckesson Medical-Surgical Inc. Corporate Office

Hylenex Injection (Mckesson) – Temperature Excursion (2024)

cGMP Deviations: Temperature excursion

Class IIModerate

FDASep 11, 2024Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Sqwincher Electrolyte Mix (Kent Precision) – Metal Contamination (2024)

Potential foreign material (metal)

Class II

1...48 495051 52...557

Page 50 of 557Next

Moderate

FDASep 9, 2024AL, ID, IL +8 more• Kent Precision Foods Group, Inc.

Sqwincher Electrolyte Mix (Kent Precision) – Metal Contamination (2024)

Potential foreign material (metal)

Class IIModerate

FDASep 9, 2024AL, ID, IL +8 more• Kent Precision Foods Group, Inc.

SONIALVISION G4 (Shimadzu) – Image Display Problem (2024)

X-ray R/F system software with certain versions of the control board may occasionally fail to display images when switching from Fluoroscopy mode to Radiography mode, which may lead to the possibility of delay or cancellation of the examination.

Moderate

FDASep 6, 2024Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

FLUOROspeed (Shimadzu) – Image Display Issue (2024)

Moderate

FDASep 6, 2024Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

Trinias Unity (Shimadzu) – Movement Interference Risk (2024)

If digital angiography system is used with a specific catheterization table and the operator directs simultaneous movement of the table and the C-arm using direct memory, then direct memory button is released, the table may continue to move, which the operator can stop by pressing the stop button.

Moderate

FDASep 6, 2024Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

Access Thyroglobulin Antibody (Beckman) – Result Accuracy Issue (2024)

IFUs for the device incorrectly states the biotin interference was remediated. The issue could result in potentially false-low results.

Low

FDASep 5, 2024Nationwide• Beckman Coulter, Inc.

1.2mm Cross Cut Fissure (Stryker) – Endotoxin Risk (2024)

May exhibit endotoxin levels greater than 2.15 EU/device, fever and inflammation may occur from endotoxin exposure and meningitis may only occur if there is contact with cerebrospinal fluid and thus, neurosurgical/spinal procedures may be considered a population at greatest risk.

Moderate

FDASep 5, 2024Nationwide• Stryker Corporation

Volkswagen ID.4 (Volkswagen) – Door Handle Electrical Issue (2024)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021-2024 ID.4 vehicles. The door handles may allow water to enter the circuit board assembly, which can cause the doors to open unexpectedly.

High

NHTSASep 4, 2024Nationwide• VOLKSWAGEN

BK Medical Ultrasound (B-K Medical) – Power Connection Risk (2024)

The internal power connections at the power inlet of the ultrasound devices can come loose resulting in the potential for excessive heat which could lead to a thermal event or the device becoming inoperable.

High

FDASep 4, 2024Nationwide• B-K Medical A/S Mileparken 34 Herlev Denmark

Insight Base Flex (Trackx) – Incorrect Expiration Label (2024)

The patient label stickers may have the wrong expiration date recorded. The contract manufacturer entered the manufacturing date (2024-04-01) as the expiration date. The actual expiration date of the product is 2027-04-01. This is reflected on the carton label and sterile pouch label correctly.

Low

FDASep 3, 2024FL, NY, NC +2 more• Trackx Technology Inc

Kilimanjaro E-Bike Carrier (Kilimanjaro) – Carrier Rack Risk (2024)

Alltrade Tools LLC (Alltrade) is recalling all Kilimanjaro E-bike racks sold at Costco and Costco.com. Please see the recall report for the model numbers and sizes. The connection points may crack, which can cause the rack to fail.

High

NHTSAAug 30, 2024Nationwide• KILIMANJARO

Trevo Trak Microcatheter (Stryker) – Packaging Label Issue (2024)

Stryker Neurovascular has observed that devices with Out of United States (OUS) approved Instructions for Use (IFU) and Packaging Labels (pouch and carton), different configurations, have been erroneously distributed to customers in the US.

Low

FDAAug 30, 2024Nationwide• Stryker Neurovascular

Mupirocin Ointment (Glenmark) – Subpotent Drug (2024)

Subpotent Drug

Class IIModerate

FDAAug 30, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Hemo-7 Hemospray (Wilson-Cook) – Raw Material Nonconformance (2024)

Specific lots of product have been manufactured with nonconforming raw materials.

Moderate

FDAAug 29, 2024Nationwide• Wilson-Cook Medical Inc.

HALO 1000 Power Stations (DBK Electronics) – Fire Hazard (2024)

Fire/Burn Risk

The portable power stations are high-capacity lithium-ion battery power banks with three USB-A charge ports, a USB-C fast charge port, three AC outputs, two DC outputs, a DC socket, an LCD display, a built-in flood light, and a collapsible handle. The following HALO 1000 Portable Power Stations are included in this recall: Product Description/Color Model Number SKU UPC Stone Gray PS-1000 801108111 840056145528 Carbon PS-1000 801108112 840056145535 Desert Sand PS-1000 801108113 840056145542 Midnight Blue PS-1000 801108114 840056145559 Woodland Green PS-1000 801108115 840056145566 The model number, SKU number and UPC are located on the bottom of the product. Units sold by QVC subject to the recall were sold under QVC item number E235474.

High

CPSCAug 29, 2024Nationwide• Shenzhen DBK Electronics Co. Ltd.,of China

Pickled Garlic (Niitakaya) – Undeclared Fish (2024)

Undeclared Allergen

Undeclared allergen (Fish) Ingredient

Class IIModerate

FDAAug 29, 2024AZ, CA, GA +5 more• Niitakaya USA Inc

Pink Pickled Garlic (Niitakaya) – Undeclared Fish (2024)

Undeclared Allergen

Undeclared allergen (Fish) Ingredient

Class IIModerate

FDAAug 29, 2024AZ, CA, GA +5 more• Niitakaya USA Inc

Volkswagen ID.4 (VOLKSWAGEN) – Air Bag Fastener Risk (2024)

Volkswagen Group of America, Inc. (VW) is recalling certain 2023-2024 ID4 vehicles. The fasteners securing the passenger frontal air bag inflator may be loose.

High

NHTSAAug 28, 2024Nationwide• VOLKSWAGEN