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Ad-Tech Medical Instrument Corporation

Ad-Tech Medical Instrument Corporation Recalls

All product recalls associated with Ad-Tech Medical Instrument Corporation.

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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 4801–4820 of 17593 recalls

Ad-Tech Lightweight CABRIO Cable (Ad-Tech) – incorrect label version (2021)

Incorrect version of labels were used.

Low

FDAAug 9, 2021Nationwide• Ad-Tech Medical Instrument Corporation

Peterbilt 348 (Custom Fire) – Emergency Vehicle Fuel Issue (2021)

Fire/Burn Risk

Custom Fire Apparatus, Inc. (Custom Fire) is recalling certain 2017-2021 Peterbilt 348, Freightliner M2, Kenworth T370, and T880 emergency vehicles equipped with Cummins L9 diesel engines. The sealing washer may not seat correctly in the pilot boreholes, allowing the high-pressure fuel rail assembly to leak.

High

NHTSAAug 6, 2021Nationwide• CUSTOM FIRE

Spartan Metrostar (Custom Fire) – Hydraulic Pressure Issue (2021)

Fire/Burn Risk

Custom Fire Apparatus, Inc. (Custom Fire) is recalling certain 2019-2021 Spartan Gladiator and Metrostar emergency vehicles. Pressure may build in the power steering pump and break the shaft seal, resulting in a loss of power steering assist.

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High

NHTSAAug 6, 2021Nationwide• CUSTOM FIRE

AMSORB PLUS Prefilled G-CAN (Armstrong Medical) – Gas Flow Resistance (2021)

Some devices may be associated with high and unexpected resistance to gas flow during clinical use, impacting or preventing adequate ventilation of an anaesthetised patient, which could cause a delay in treatment. Not all defective canisters will be identified by the pre-use test.

Moderate

FDAAug 5, 2021Nationwide• Armstrong Medical Services Limited NewBridge Road Wattstown Business Park Coleraine Ireland

Access SARS CoV-2 IgG Assay (Beckman Coulter) – EUA Evidence Issue (2021)

Firm's submission for Emergency Use Authorization (EUA) contained insufficient evidence to be granted EUA Authorization to distribute

Moderate

FDAAug 5, 2021Nationwide• Beckman Coulter Inc.

Ultrasound Gel (Mac Medical) – Bacterial Contamination (2021)

Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.

High

FDAAug 4, 2021Nationwide• Mac Medical Supply Co Inc

SARS-CoV-2 Test (Roche) – False Positive Results (2021)

Customers have reported an increased number of false positive SARS-CoV-2 results.

High

FDAAug 4, 2021Nationwide• Roche Molecular Systems, Inc.

Mr. Heater Propane Regulator (Enerco) – Equipment Defect (2021)

Fire/Burn Risk

Enerco Group, Inc. is recalling certain Enerco and Mr. Heater propane regulators with model numbers 73766 and 73836(G). Please see attached model listing for all affected part numbers. The LP regulator that controls the LP gas pressure may fail, allowing excessive gas pressure that causes the appliance flame to increase.

High

NHTSAAug 4, 2021Nationwide• ENERCO/ MR. HEATER

Arc Endocuff Vision (Olympus) – Packaging Sterility Breach (2021)

Packaging seal defect may allow a breach of the package sterile barrier and result in patient infection.

Moderate

FDAAug 3, 2021Nationwide• Olympus Corporation of the Americas

Clopidogrel Tablets (Macleods) – Foreign Matter (2021)

Presence of foreign matter

Class IIModerate

FDAAug 2, 2021Nationwide• Macleods Pharma Usa Inc

Arjo Disposable Repositioning Sling (Antigua) – Trip Hazard (2021)

Sling loop straps on device pose a trip hazard.

Moderate

FDAJul 30, 2021Nationwide• Antigua Carretera Sanchez Itabo, Haina Dominican Republic (the)

BOND CDX2 Antibody (Leica) – Performance Specification Issue (2021)

Product may not perform as specified in IFU.

Moderate

FDAJul 30, 2021Nationwide• Leica Microsystems, Inc.

Fludarabine Injection (Custopharm) – Sterility Concern (2021)

Lack of Assurance of Sterility: the manufacturing firm had microbial recoveries during environmental monitoring in aseptic areas of manufacturing.

Class IIModerate

FDAJul 30, 2021Nationwide• Custopharm, Inc.

Succinylcholine Chloride (BayCare) – Sterility Risk (2021)

Lack of sterility assurance

Class IIModerate

FDAJul 30, 2021FL• BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy

OASIS MRI System (Hitachi) – Rubber Material Undeclared (2021)

There was no label on the pad packaging or notification in the user manual that the table pads contained dry natural rubber which is required by the Code of Federal Regulations section 21CFR801.437.

Moderate

FDAJul 29, 2021Nationwide• Hitachi Healthcare Americas Corporation

Portable Generators (Generac) – Amputation Risk (2021)

This recall involves 6500 watt and 8000 watt Generac portable generators with unit type numbers XT8000E, XT8000EFI, GP6500, GP6500E, GP8000E and HomeLink 6500E portable generators, and DR models PRO 6500M and PRO 6500E portable generators. The generators have gasoline-powered engines that are used to generate electricity for use as backup power. The portable generators have two-wheels and a single, U-shaped, two-grip, flip-up pin-lock handle to help move the generator. Only the generators listed below are included in this recall. The unit type is identified on the front of the product. The model and serial numbers are printed on a label on the product. Consumers can also check specific unit type, model number, and serial number location information at www.generac.com/service-support/product-support-lookup Unit Type Model Number First Serial Number Last Serial Number XT8000E G0064330 G0064331 3000037849 3005569372 G0064340 G0064342 XT8000EFI G0071620 G0071621 3003336356 3006597843 G0071621R GP6500 G0076720 G0076800 G0076800R G0076812 G0076830 G0076830R G0076902 G0076902R G0076903 GP6500E G0076820 G0076820R G0076822 GP8000E G0076731 G0076751 G0076751R G0076761 G0076761R G0076861 G0076861R PRO 6500M GP16505DMN GP16505DMNR PRO 6500E GP16505DEN HomeLink 6500E G0068650 G0068651 G0079960

Moderate

CPSCJul 29, 2021Nationwide• Generac Power Systems, of Waukesha, Wis.

ECHELON Oval MRI System (Hitachi) – Rubber Material Undeclared (2021)

There was no label on the pad packaging or notification in the user manual that the table pads contained dry natural rubber which is required by the Code of Federal Regulations section 21CFR801.437.

Moderate

FDAJul 29, 2021Nationwide• Hitachi Healthcare Americas Corporation

ECHELON MRI System (Hitachi) – Rubber Material Undeclared (2021)

There was no label on the pad packaging or notification in the user manual that the table pads contained dry natural rubber which is required by the Code of Federal Regulations section 21CFR801.437.

Moderate

FDAJul 29, 2021Nationwide• Hitachi Healthcare Americas Corporation

Ethosuximide Oral Solution (PAI Holdings) – CGMP Violation (2021)

Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.

Class IIModerate

FDAJul 29, 2021Nationwide• PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Cimetidine Hydrochloride (PAI Holdings) – CGMP Violation (2021)

Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.

Class IIModerate

FDAJul 29, 2021Nationwide• PAI Holdings, LLC. dba Pharmaceutical Associates Inc