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Olympia Compounding Pharmacy dba Olympia Pharmacy

Olympia Compounding Pharmacy dba Olympia Pharmacy Recalls

All product recalls associated with Olympia Compounding Pharmacy dba Olympia Pharmacy.

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

Most Recent

Dec 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 2461–2480 of 10937 recalls

Lipostat Plus SF (Olympia Pharmacy) – Sterility Concerns (2022)

Lack of assurance of sterility.

Class IIModerate

FDAMay 9, 2022Nationwide• Olympia Compounding Pharmacy dba Olympia Pharmacy

Olympia Mineral Blend (Olympia Pharmacy) – Sterility Risk (2022)

Lack of assurance of sterility.

Class IIModerate

FDAMay 9, 2022Nationwide• Olympia Compounding Pharmacy dba Olympia Pharmacy

GreenSpeed Magnum Recumbent Trike (WizWheelz) – Crash Risk (2022)

This recall involves GreenSpeed Magnum and Magnum XL model recumbent trikes with Sturmey-Archer drum brake quick release front axles. Magnum or Magnum XL are printed on the trikes. Sturmey-Archer is printed on the hub/wheel where the axle is attached. Serial numbers P21276160 through P21460262 are included in this recall. The recalled trikes are orange, blue or charcoal in color with a black seat and three wheels. The serial numbers are printed on the left dropout, which is a slot in the rear of the bike where the rear wheel attaches. Consumers can check their serial numbers at https://greenspeed-trikes.com/wp-content/uploads/2022/04/GreenSpeed-Magnum-Magnum-XL-Axle-Recall-Serial-Numbers-UPDATED.pdf

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Moderate

CPSCMay 5, 2022Nationwide• WizWheelz Inc., of Grand Rapids, Michigan

Alphenix 4D CT System (Canon) – Operational Restriction (2022)

CT operation may be restricted by an interlock which is a result of an system error and the CT system may stop operating properly after an attempt to cancel the error message has been initiated.

Moderate

FDAMay 3, 2022CA, CO, FL +2 more• Canon Medical System, USA, INC.

NIM Vital Interface (Medtronic) – Software Anomaly (2022)

Software anomaly was identified.

Moderate

FDAMay 3, 2022Nationwide• Medtronic Xomed, Inc.

NIM Vital Console (Medtronic) – Software anomaly (2022)

Software anomaly was identified.

Moderate

FDAMay 3, 2022Nationwide• Medtronic Xomed, Inc.

COVID-19 Collection Tray (American Contract) – assembly training (2022)

Affected products were assembled off-site by individuals who may not have been properly trained.

Moderate

FDAMay 2, 2022IN, MN• American Contract Systems, Inc.

Clean Catch Urine Kit (American Contract) – assembly training (2022)

Affected products were assembled off-site by individuals who may not have been properly trained.

Moderate

FDAMay 2, 2022IN, MN• American Contract Systems, Inc.

NIM CONTACT EMG Tube (Medtronic) – airway obstruction (2022)

The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

Moderate

FDAApr 29, 2022Nationwide• Medtronic Xomed, Inc.

NIM EMG Endotracheal Tube (Medtronic) – airway obstruction (2022)

The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

Moderate

FDAApr 29, 2022Nationwide• Medtronic Xomed, Inc.

1 Series CX Phototherapy (Daavlin) – calibration software issue (2022)

Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

Moderate

FDAApr 26, 2022Nationwide• Daavlin Distributing Company

4 Series CX Phototherapy (Daavlin) – calibration software issue (2022)

Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

Moderate

FDAApr 26, 2022Nationwide• Daavlin Distributing Company

INTERTAN Nail (Smith & Nephew) – left-right labeling error (2022)

Right nails were anodized, marked, and labelled as left nails and vice versa

Moderate

FDAApr 22, 2022Nationwide• Smith & Nephew Orthopaedics GmbH Alemannenstr. 14 Tuttlingen Germany

Nectar Premier Mattresses (Elite Comfort Solutions) – flammability issue (2022)

Fire/Burn Risk

This recall involves certain Nectar Premier Mattresses manufactured on two specific dates: King size: manufactured on 9/24/2021; and Queen size: manufactured on 9/27/2021. The recalled mattresses have a white poly-blend top cover with black side panels and a vertical purple sash, and the foot of the mattresses is marked with the large (13" long, 2" tall) embroidered "nectar" logo and the word "Nectar" imprinted in white, and also have the date of manufacture on the white tag. Elite Comfort Solutions, the date of manufacture in MM/DD/YY format (9/24/21 for king mattresses or 9/27/21 for queen mattresses), the model number, CHILL and "Prototype ID:ECS2003RHCH" can be found on the bottom portion of the white tag which is located at the head of the mattress.

High

CPSCApr 21, 2022Nationwide• Elite Comfort Solutions LLC, of Newnan, Georgia

ProudP Uroflow Tracker (Dain Technology) – sound processing issue (2022)

Due to interference with the Live Listen feature of hearing aid or AirPods, the user's iPhone may perform automatic processing of the urination sound signal, resulting in lower urination volume and velocity values than expected.

Low

FDAApr 21, 2022Nationwide• Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) Seocho-Daero, Seocho # 413 398 Platinum Tower Seoul Korea (the Republic of)