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Samsung Electronics America Inc., of Ridgefield Park, N.J.

Samsung Electronics America Inc., of Ridgefield Park, N.J. Recalls

All product recalls associated with Samsung Electronics America Inc., of Ridgefield Park, N.J..

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Recall Summary

Total Recalls

709

Past Year

Class I (Serious)

Most Recent

Nov 2025

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 61–80 of 709 recalls

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

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

Sevoflurane E_Vap.(Quik-Fil):used with the A9 Anesthesia ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention

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FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Desflurane E_Vap.(Saf-T-Fill) used with the A9 Anesthesia... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Isoflurane E_Vap.(Safety Filling adapter): used with the ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Sevoflurane E_Vap.(Safety Filling adapter) used with the ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Everest Bipolar Cutting Forceps (Olympus) – Packaging Breach (2024)

Fractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach

FDAJul 1, 2024Nationwide• Olympus Corporation of the Americas

ESG-410 Electrosurgical Generator (Olympus) – Power-On Failure (2024)

Electrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or prolonged surgery

FDAJun 21, 2024Nationwide• Olympus Corporation of the Americas

Soltive Pro Laser System (Olympus) – Footswitch Pairing Issue (2024)

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

FDAMay 31, 2024Nationwide• Olympus Corporation of the Americas

Soltive Premium Laser System (Olympus) – Footswitch Pairing Issue (2024)

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

FDAMay 31, 2024Nationwide• Olympus Corporation of the Americas

Soltive Laser Wireless Footswitch (Olympus) – Pairing Problem (2024)

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

FDAMay 31, 2024Nationwide• Olympus Corporation of the Americas

EasySuite 4K Operating Room System (Olympus) – Testing Records (2024)

A subset of the ES4K systems do not have complete records for earth leakage testing. The earth leakage test is a series of measurements intended to confirm that the amount of electrical current flowing to the earth is within standard limits

FDAApr 24, 2024Nationwide• Olympus Corporation of the Americas

OES 4000 Hysteroscope (Olympus) – leakage test omission (2024)

The required leakage test was not performed following of a re-work for a non-conformity. This could potentially result in liquid ingress into the eyepiece and cause a foggy image.

FDAApr 18, 2024Nationwide• Olympus Corporation of the Americas

Noblus AC Adapter (Fujifilm) – power socket overheat (2024)

AC adapters of Noblus can heat up, and cause smoke in the worst case, when an excessive mechanical stress is applied to the socket for power cable (frequent insertion/removal of the power cable).

FDAApr 11, 2024Nationwide• FUJIFILM Healthcare Americas Corporation

FDR Visionary Suite (Fujifilm) – tube support risk (2024)

Bolts on the CH-200 tube may rupture due to fatigue failure, causing the tube support to fall, could result in patient injury

FDAApr 11, 2024Nationwide• FUJIFILM Healthcare Americas Corporation

InstaClear Lens Sheath (Olympus) – Potential Breakage (2024)

Potential for distal end of the sheath to break off during a procedure.

FDAApr 3, 2024Nationwide• Olympus Corporation of the Americas

PowerSeal 44cm Curved Jaw Sealer (Olympus) – Incomplete Seal Cycle (2024)

Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.

FDAMar 7, 2024Nationwide• Olympus Corporation of the Americas

PowerSeal 5mm Curved Jaw Sealer (Olympus) – Incomplete Seal Cycle (2024)

FDAMar 7, 2024Nationwide• Olympus Corporation of the Americas

PowerSeal 37cm Curved Jaw Sealer (Olympus) – Incomplete Seal Cycle (2024)

FDAMar 7, 2024Nationwide• Olympus Corporation of the Americas

Triangle Tip Electrosurgical Knives (Olympus) – Breakage Warning (2024)

Due to increase in complaints for the KD-640L and KD-645L Triangle Tip Electrosurgical Knives breaking off during use -issuing reminder to users to utilize the electrosurgical knife in accordance with the Instructions for Use, which details critical specifications regarding electrosurgical unit compatibility and output due to reports of serious injury

FDAMar 1, 2024Nationwide• Olympus Corporation of the Americas

Soltive Pro Laser (Olympus) – Non-Compliant Power Cord (2024)

A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.

FDAJan 29, 2024IN• Olympus Corporation of the Americas