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
/
Essential Medical Supply, Inc.

Essential Medical Supply, Inc. Recalls

All product recalls associated with Essential Medical Supply, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 22241–22260 of 25000 recalls

Essential Medical Supply, Inc.: Essential Medical Supply brand Essential Rollator with Lo...

The caster may separate from the frame completely causing injury to the user.

FDAMay 8, 2009Nationwide• Essential Medical Supply, Inc.

Abiomed, Inc.: Abiomed AB5000 Portable Driver Catalog number: 0025-0000...

The Emergency System Operation (ESO) mode may not provide adequate patient support under a specific operating condition.

FDAMay 8, 2009AL, FL, IN +3 more• Abiomed, Inc.

GE Medical Systems, LLC: Datex-Ohmeda S/5 Device Interfacing Solution, N-DISVENT 0...

GE Healthcare has recently become aware of an issue in the calculations associated with Datex-Ohmeda S/5 Device Interfacing Solution N-DISVENT-02 interfaced between certain Datex-Ohmeda patient monitors (Datex-Ohmeda S/5 Anesthesia Monitor (AM), Datex-Ohmeda S/5 Critical Care Monitor (CCM), Datex-Ohmeda S/5 Compact Anesthesia Monitor (CAM), Datex-Ohmeda S/5 Compact Critical Care Monitor (CCCM)) an

1...1111 111211131114 1115...1250

Page 1113 of 1250Next

FDAMay 8, 2009AL, AK, AZ +34 more• GE Medical Systems, LLC

Off-Road Motorcycles (KTM) – Front Fork Failure (2009)

This recall involves model year 2009 KTM off-road motorcycles. The model name and KTM™ logo are located on the right and left shrouds. The following models are included in this recall:Model Name Description 125SX Orange / Black 150SX Orange / Black 250XC-W Orange / Black 300XC-W Orange / Black

CPSCMay 7, 2009Nationwide• KTM North America Inc., of Amherst, Ohio

Whatman, Inc.: Whatman Body Fluid Collection Paper 903 The device is us...

The two portions of the card are coming apart prematurely.

FDAMay 6, 2009Nationwide• Whatman, Inc.

Torcofix/Torcoflex Torque Wrenches (Richard Abraham Herder) – Injury Risk (2009)

The wrenches were sold under three styles names: Richard Abraham Herder KG "Gedore/Rahsol" label, the Mountz "Titan" label, and the Mountz "Erico" label. Only wrenches with the serial numbers within the following ranges are included in the recall: From serial no. To serial no. 1268368 1341104 A003977 A039760 B000493 B032301 C000001 C017795 E000001 E020205 F000001 F013249 H000001 H000128 2174340 2230753 Recalled wrenches include the following product/brand names and model numbers: Product/Brand Name Model Nos. GEDORE/RAHSOL TORCOFIX K with Ratchet 4550-10; 4550-20; 4550-30; 4550-40 GEDORE/RAHSOL TORCOFLEX K with Ratchet 3550-07; 3550-10; 3550-20; 3550-30; 3550-2006 GEDORE/RAHSOL TORCOFIX Z with Spigot 4410-01; 4420-01; 4430-01; 4440-01 GEDORE/RAHSOL TORCOFIX SE with rectangle holder 4100-01; 4200-02; 4201-01; 4300-01; 4301-01 GEDORE/RAHSOL TORCOFIX K US with Ratchet 6550-15; 6551-07; 6551-10; 6551-30; 6551-60 MOUNTZ TITAN with Ratchet 280012; 280013; 280014 MOUNTZ TITAN with Spigot 280022; 280023; 280024 MOUNTZ ERICO ELT110D with Ratchet ELT110D The serial number is printed on the side of every torque wrench and the model number is printed on the label on the front and the back of the steel tube.

CPSCMay 6, 2009Nationwide• Richard Abraham Herder KG, of Solingen, Germany

Erwin and Poseidon Beanie Hats (Ambler Mountain Works) – Choking Hazard (2009)

Choking Hazard

The Erwin Beanie is primarily green and white yarn knitted to configure a frog with white eyeballs and a red smile. The Poseidon Beanie comes in several colors of yarn and has hand sewn turtles, whales and octopus attached to the beanie. The beanies have the firm's logos "Ambler" or "A" printed on a fabric tag.

CPSCMay 5, 2009Nationwide• Ambler Mountain Works, of Canmore, Alberta, Canada

GE Medical Systems, LLC: GE Healthcare, CT Perfusion 4 on Advantage Workstation, C...

GE Healthcare has recently become aware of the need to adjust default settings associated with the use of CT Perfusion 4 on the Advantage Workstation, ST and PET/CT consoles that may impact patient safety. The default parameter settings in CT Perfusion 4 may not be optimal in the case of data acquired with longer time sampling intervals such as axial scans with inter scan delay (ISD) greater th

FDAMay 4, 2009AZ, CA, CT +17 more• GE Medical Systems, LLC

NRT Nordisk Rontgen Teknik A/S Birkegaardsvej 16 Hasselager Denmark: Celex/GE Precision MPi, REF no.: 02980000 Is an all-digi...

The GE Precision MPi is in violation with 21 CFR Part 1020.32 requiring a signal audible to the fluoroscopist to sound for each passage of 5 minutes of fluoroscopic irradiation time during an examination or procedure.

FDAMay 1, 2009Nationwide• NRT Nordisk Rontgen Teknik A/S Birkegaardsvej 16 Hasselager Denmark

GE Medical Systems, LLC: HiSpeed X/i Computed Tomography operator consoles with th...

It was discovered that the operator console did not have a label affixed in accordance with 21CFR 1010.2 indicating certification to applicable performance standards.

FDAMay 1, 2009AL, CA, CT +9 more• GE Medical Systems, LLC

Kamiya Biomedical Company, LLC: "K-ASSAY CRP (3) Calibrator E". This product is an IVD ...

The long-term stability of level 2 (1.0 mg/dL) may not be within the specifications due to a decrease in CRP concentration.

FDAMay 1, 2009Nationwide• Kamiya Biomedical Company, LLC

Philips Medical Systems North America Co. Phillips: The product's marketing brochure states: "1.5T coils and ...

Fire/Burn Risk

Combined use of the Synergy Flex-M / Shoulder Coil 1.5T increases the chance of RF interaction and heating up of the coil. This may result in possible burns of the patient.

FDAMay 1, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Disetronic Medical Systems, Inc.: Roche ACCU-CHEK Spirit insulin pump. Part numbers 454049...

The "up" and "down" buttons, which are used for changing the program in the menu or to administer additional insulin through a bolus delivery, may experience intermittent failure or completely cease to operate.

FDAApr 30, 2009Nationwide• Disetronic Medical Systems, Inc.

Philips Medical Systems (Cleveland) Inc: Dental Application on the Extended Brilliance Workspace v...

Philips Healthcare has decided to recall the Dental Application on the Extended Brilliance Workspace v4.0 and v4.0.1 due to the fact that when images are saved or filmed that contain the Curved Multi-planar Reformation Section (cMPRS) views that were created with a short curve the Right/Left annotations will be reversed.

FDAApr 27, 2009AL, AZ, AR +22 more• Philips Medical Systems (Cleveland) Inc

Leg Curl Machines (Paramount Fitness) – Crushing Hazard (2009)

Laceration Risk

This recall involves the Paramount Fitness PL2100 leg curl machine. The single station weight machine is designed to exercise the hamstring muscles. Serial numbers involved in this recall include: PL21-9301-000 through PL21-9510-099. The serial number is printed on the back of the weight stack frame on the lower right. Model number PL2100 is printed on the exercise procedure label on the front of the machine. The Paramount Fitness logo is printed vertically on the frame.

CPSCApr 27, 2009Nationwide• Paramount Fitness Corp., of Los Angeles, Calif.

Abiomed, Inc.: iPulse Circulatory Support System Catalog number: 0036-0...

iPulse Console SC1035 displayed a "Low Pressure / Low Flow" alarm and stopped pumping during patient transport in battery operation.

FDAApr 23, 2009AR, CA, CT +19 more• Abiomed, Inc.

OPTI Medical Systems, Inc: OPTI LION Cassettes, E-Plus, Model BP7507 (25 per box), O...

Outer box labeling shows an incorrect storage temperature range.

FDAApr 20, 2009Nationwide• OPTI Medical Systems, Inc

Spinal Elements, Inc: Mercury Spinal System DIA 5.5 x 30 MM Lordosed Rod, Part...

Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.

FDAApr 17, 2009IN, OH, PA• Spinal Elements, Inc

Patterson Medical Holdings, Inc.: Leckey 4-Point Pelvic Harness Belts, catalog 081326990; J...

The plastic buckles on the hip belts of the 4-Point Pelvic Harness may break.

FDAApr 17, 2009Nationwide• Patterson Medical Holdings, Inc.

Spinal Elements, Inc: Mercury Spinal System DIA 5.5 x 400mm Straight Rod, Part...

Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.

Class IIILow

FDAApr 17, 2009IN, OH, PA• Spinal Elements, Inc