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SEER MEDICAL PTY LTD 278-284 Queensberry St Melbourne Australia

SEER MEDICAL PTY LTD 278-284 Queensberry St Melbourne Australia Recalls

All product recalls associated with SEER MEDICAL PTY LTD 278-284 Queensberry St Melbourne Australia.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 1861–1880 of 21320 recalls

Seer Home EEG System (Seer Medical) - EMC Assessment Gap (2024)

During CAPA investigations of sight production inconsistencies, it was highlighted that previous Electromagnetic Compatibility (EMC) assessments related to RF radiated emissions may not be reasonably equivalent to the current product due to design changes in the system. A new CAPA was opened to investigate the radiated emissions compliance issues. - Seer Home Systems distributed and retained in the field were not compliant with Electromagnetic Compatibility (EMC) testing according to IEC 60601-1-2 - Seer Home Systems, including accessories, were manufactured and distributed without application of proper design change and manufacturing controls - Seer Home Systems were distributed with labeling deficiencies

High

FDAAug 12, 2024Nationwide• SEER MEDICAL PTY LTD 278-284 Queensberry St Melbourne Australia

Prelude Sheath Introducer (Merit Medical) - Incorrect Size Labeling (2024)

7F sheath introducers labeled as 7.5F

Moderate

FDAAug 12, 2024Nationwide• Merit Medical Systems, Inc.

1...92 939495 96...1066

Page 94 of 1066Next

BD FACSDuet Preparation System (BD) - Sample Dispensing Error (2024)

Sample preparation system with software may cause: 1) Multidispense feature enabled with 2-tube assay: Specimen volume dispensed into tube1 at least 3% higher than volume in tube2, or 2) Absolute counts calculated using Trucount Tubes: increased volume in tube1 may result in 20% higher absolute counts in tube 1 than tube 2; could result in additional blood collection, delayed results/patient therapy.

Moderate

FDAAug 12, 2024AK, CA, ID +10 more• Becton, Dickinson and Company, BD Bio Sciences

Custom Procedure Kit (Merit Medical) - Incorrect Size Labeling (2024)

7F sheath introducers labeled as 7.5F

Moderate

FDAAug 12, 2024Nationwide• Merit Medical Systems, Inc.

ViewPoint Imaging System (GE Healthcare) - Cybersecurity Vulnerability (2024)

The National Institute of Standards and Technology (NIST) has identified in the National Vulnerability Database (NVD) that NexGen Healthcare Mirth Connect, prior to version 4.4.1, has a potential vulnerability allowing the deserialization of untrusted data (CVE-2023-43208). Mirth products may have been installed and configured with your ViewPoint / ViewPoint 6 system by GE HealthCare. This vulnerability could allow a malicious actor to access the system and potentially manipulate patient data.

High

FDAAug 8, 2024Nationwide• GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

Anesthesia Extension Set (B. Braun) - Connector Leakage Risk (2024)

Potential for product leakage from the Spin Lock Connector on the distal end of the device due to the migration of excess solvent during the assembly process.

Moderate

FDAAug 8, 2024Nationwide• B. Braun Medical, Inc.

Philips Allura Xper System (Philips) - Bolt Placement Error (2024)

A half-threaded bolt was included in the LTE kits instead of the correct full-threaded bolt.

Moderate

FDAAug 8, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Slide-In Electric Ranges (Samsung) – Fire Hazard (2024)

Fire/Burn Risk

This recall involves Samsung Electric Slide-In Ranges with the model numbers below. The model number is located on the ranges on the inside upper left corner of the oven door or inside the storage bin located on the bottom of the oven. Recalled Model Numbers NE58K9430SS/AA NE58N9430SG/AA NE58R9431SG/AA NE58R9431SS/AA NE58R9431ST/AA NE58F9500SS/AA NE58K9500SG/AA NE58F9710WS/AA NE58K9850WS/AA NE58K9850WG/AA NE58K9852WG/AA NE58H9950WS/AA NE58R9311SS/AA NE63T8111SG/AA NE63T8111SS/AA NE63T8311SG/AA NE63T8311SS/AA NE63BG8315SSAA NE63CB831512AA NE63BB851112AA NE63T8511SG/AA NE63T8511SS/AA NE63T8511ST/AA NE63A8711QN/AA NE63BB871112AA NE63T8711SG/AA NE63T8711SS/AA NE63T8711ST/AA NE63T8751SG/AA NE63T8751SS/AA

High

CPSCAug 8, 2024Nationwide• Samsung Electronics America Inc., of Ridgefield Park, N.J.

Buick All-Weather Floor Liner (Buick) - Installation Risk (2024)

General Motors, LLC (GM) is recalling certain Buick Envision all-weather floor mats with part number 85647097, that may have been installed in certain 2024 Buick Envision vehicles. The accelerator pedal may become trapped under the floor mat, which can result in unintended acceleration.

High

NHTSAAug 8, 2024Nationwide• BUICK

Blood Pressure Module BPM3 (Fresenius) - Measurement Recording Issue (2024)

Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor TM-2917B with firmware version S005) will not record Blood Pressure measurements and does not alarm if the cuff tubing is kinked close to the cuff.

Moderate

FDAAug 8, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Testosterone Gel (Teva) – Superpotent Medication (2024)

Superpotent Drug

Class IIModerate

FDAAug 8, 2024Nationwide• Teva Pharmaceuticals USA, Inc

Ibuprofen Tablets (Preferred Pharmaceuticals) – Impurity Issues (2024)

Failed Impurities/Degradation Specifications - at 18-month Stability testing

Class IIModerate

FDAAug 8, 2024CA, NV• Preferred Pharmaceuticals, Inc.

ViewPoint 6 System (GE Healthcare) - Cybersecurity Vulnerability (2024)

High

FDAAug 8, 2024Nationwide• GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

Neuro Vascular Kit (American Contract) - Humidity Control Failure (2024)

ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

Moderate

FDAAug 7, 2024Nationwide• American Contract Systems, Inc.

Some automated in vitro diagnostic modules and instruments manufactured or serviced between May 2022 and May 2024 were calibrated with internal equipment that may lead modules and instruments to report higher melting temperatures, which may lead to erroneous results including false positive Salmonella, Giardia lamblia, false positive/negative Norovirus, and false negative MRSA.

Moderate

FDAAug 7, 2024Nationwide• BioFire Diagnostics, LLC

IR Procedure Pack (American Contract) - Humidity Control Failure (2024)

Moderate

FDAAug 7, 2024Nationwide• American Contract Systems, Inc.

Stay Informed

SEER MEDICAL PTY LTD 278-284 Queensberry St Melbourne Australia Recalls

Recall Summary

Seer Home EEG System (Seer Medical) - EMC Assessment Gap (2024)

Prelude Sheath Introducer (Merit Medical) - Incorrect Size Labeling (2024)

BD FACSDuet Preparation System (BD) - Sample Dispensing Error (2024)

Custom Procedure Kit (Merit Medical) - Incorrect Size Labeling (2024)

ViewPoint Imaging System (GE Healthcare) - Cybersecurity Vulnerability (2024)

Anesthesia Extension Set (B. Braun) - Connector Leakage Risk (2024)

Philips Allura Xper System (Philips) - Bolt Placement Error (2024)

Slide-In Electric Ranges (Samsung) – Fire Hazard (2024)

Buick All-Weather Floor Liner (Buick) - Installation Risk (2024)

Blood Pressure Module BPM3 (Fresenius) - Measurement Recording Issue (2024)

Testosterone Gel (Teva) – Superpotent Medication (2024)

Ibuprofen Tablets (Preferred Pharmaceuticals) – Impurity Issues (2024)

ViewPoint 6 System (GE Healthcare) - Cybersecurity Vulnerability (2024)

Neuro Vascular Kit (American Contract) - Humidity Control Failure (2024)

Cysto FTCY03L (American Contract Systems) – Humidity Issue (2024)

Endovascular AAA Pack (American Contract) - Humidity Control Failure (2024)

Vaginal Delivery ASDV25B (American Contract Systems) – Humidity Issue (2024)

Open Shoulder LWOS39L (American Contract Systems) – Humidity Issue (2024)

FilmArray 2.0 Instrument (BioFire) - Calibration Equipment Problem (2024)

IR Procedure Pack (American Contract) - Humidity Control Failure (2024)