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
/
ASP Global, LLC. dba Anatomy Supply Partners, LLC.

ASP Global, LLC. dba Anatomy Supply Partners, LLC. Recalls

All product recalls associated with ASP Global, LLC. dba Anatomy Supply Partners, LLC..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 1401–1420 of 37661 recalls

SAFE-T-FILL Capillary (ASP Global) – False Positive Results (2025)

All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when used with Magellan Diagnostics LeadCare Testing Systems. False positive lead results may cause delayed results and additional unnecessary testing.

Moderate

FDAMay 5, 2025Nationwide• ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Access Testosterone Assay (Beckman Coulter) – Maintenance Error (2025)

Inadequate preventative maintenance (PM) performed on the scales of the RPL5 fill line, led to splashing (cross-contamination) between the wells of testosterone reagent packs lot 538081, which could potentially result in up to a 34% increase or a 23% decrease in patient results.

Moderate

FDAMay 5, 2025FL• Beckman Coulter, Inc.

Campsite Reserve (Forest River) – Solar Controller Wiring (2025)

Fire/Burn Risk

Forest River, Inc. (Forest River) is recalling certain 2025 Campsite Reserve travel trailers. The solar controller may be wired incorrectly without over current circuit protection.

1...69 707172 73...1884

Page 71 of 1884Next

Moderate

NHTSAMay 2, 2025Nationwide• FOREST RIVER

BD BBL CultureSwab (Copan) – Swab Breakage Risk (2025)

Swabs for specimen collection may be prone to breakage during product usage.

Moderate

FDAMay 2, 2025Nationwide• Copan Italia Via Francesco Perotti 10

Pre-filled Water Syringe (Healthmark) – Contamination Risk (2025)

During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their investigation. Healthmark Industries conducted its own investigation and concluded that the Pre-filled Water Syringe had been improperly used outside of the intended purpose.

Moderate

FDAMay 2, 2025Nationwide• Healthmark Industries Co., Inc.

Altec Aerial Device (Altec) – Fuel System Defect (2025)

Fire/Burn Risk

Altec Industries, Inc. (Altec) is recalling certain 2022-2024 TA Series, AT Series, L Series, LR Series Aerial Devices, and AF Series Forestry bodies. The fuel lines may not be properly secured, which can cause the lines to chafe and result in a fuel leak.

High

NHTSAMay 2, 2025Nationwide• ALTEC

ChannelCheck Pack (Healthmark) – Contamination Risk (2025)

Moderate

FDAMay 2, 2025Nationwide• Healthmark Industries Co., Inc.

Drill Stop Kit (Implant Direct) – Incorrect Components (2025)

The Drill stop kit contains incorrect components.

Moderate

FDAMay 1, 2025Nationwide• Implant Direct Sybron Manufacturing LLC

Entegra Launch (Entegra) – Incorrect Outlet Installation (2025)

Jayco, Inc (Jayco) is recalling certain 2025 Entegra Launch and Jayco Terrain motorhomes. An incorrect standard outlet was installed in the kitchen instead of a GFCI protected outlet.

High

NHTSAMay 1, 2025Nationwide• ENTEGRA

BX2 Needle Guide (Civco) – Probe Packaging Breach (2025)

During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place.

Moderate

FDAMay 1, 2025GA• Civco Medical Instruments Co. Inc.

Kodiak (Keystone) – Fold-Down Support Failure (2025)

Keystone RV Company (Keystone) is recalling certain 2025 Kodiak 2900FKSP and 308BHSL travel trailers. The struts may not support enough of the fold-down patio's weight while being raised or lowered.

Moderate

NHTSAMay 1, 2025Nationwide• KEYSTONE

Sample Probe (Beckman Coulter) – Manufacturing Defect (2025)

A manufacturing defect in the sample probe (S probe). The corners of the tip of the defective S probe are rounded and chamfered, which can prevent the proper formation of the "air layer" required for normal dispensing. The air layer is the air space that separates the cleaning water filled in the probe from the sample sucked into the probe. Maintaining this air space prevents the cleaning water and the sample from mixing. In the defective S probe, the "air layer" was not properly formed, causing the cleaning water and the sample to mix diluting the sample. As a result, the sample mixture dispensed into the cuvette has a lower concentration than the original sample, and the analyte concentration measured is lower than expected results.

Moderate

FDAApr 30, 2025Nationwide• Beckman Coulter Mishima K.K. 454-32 Higashino; Nagaizumi-Cho Sunto-Gun Japan

Cardiohelp System Wall Holder (Maquet) – Mounting Risk (2025)

HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.

High

FDAApr 30, 2025IL, MO• Maquet Cardiopulmonary Ag Kehler Str. 31 Rastatt Germany