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Ideal Specialty Apothecary, Inc. dba Ideal Pharmacy

Ideal Specialty Apothecary, Inc. dba Ideal Pharmacy Recalls

All product recalls associated with Ideal Specialty Apothecary, Inc. dba Ideal 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 2681–2700 of 10937 recalls

Medroxyprogesterone Injection (Ideal Pharmacy) – Sterility Risk (2021)

Lack of Assurance of Sterility

Class IIModerate

FDADec 21, 2021Nationwide• Ideal Specialty Apothecary, Inc. dba Ideal Pharmacy

Flat Panel Detector (Canon Medical) – Image Display Problem (2021)

Abnormal images such as horizontal stripes may be displayed and recovery may not not be possible by restarting the system. The worst case scenario is an operator who is working without a workable image may remove a catheter from the patient's blood vessel and damage the blood vessel.

Moderate

FDADec 20, 2021Nationwide• Canon Medical System, USA, INC.

Vitamin B Complex (Professional Complementary Health) – Undeclared niacin (2021)

Undeclared Allergen

1...133 134135136 137...547

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Product recalled due to undeclared niacin.

Class IIModerate

FDADec 20, 2021Nationwide• Professional Complementary Health Formulas, LLC

Inositol (Professional Complementary Health) – Undeclared niacin (2021)

Undeclared Allergen

Product recalled due to undeclared niacin.

Class IIModerate

FDADec 20, 2021Nationwide• Professional Complementary Health Formulas, LLC

Sorin Centrifugal Pump (LivaNova) – Missing Ferrite Ring (2021)

One ferrite ring expected to be installed on centrifugal pump system power cable may not be present.

Moderate

FDADec 17, 2021FL, IN, NE +1 more• LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany

Bransist Safire Digital Angiography (Shimadzu) – X-Ray Radiation Exposure (2021)

Due to the inadequate adjusting criteria in installation, the system generator on two Digital Angiography Systems, the irradiated x-ray may exceed the x-ray radiation dose rate in fluoroscopic mode.

Moderate

FDADec 16, 2021CA, FL, GA +12 more• Shimadzu Medical Systems

Shimadzu Trinias Digital Angiography (Shimadzu) – X-Ray Radiation Exposure (2021)

Due to the inadequate adjusting criteria in installation, the system generator on two Digital Angiography Systems, the irradiated x-ray may exceed the x-ray radiation dose rate in fluoroscopic mode.

Moderate

FDADec 16, 2021CA, FL, GA +12 more• Shimadzu Medical Systems

Medtronic IPC Software (Medtronic) – Authentication Issue (2021)

As a result of Medtronic's integrated power console (authentication number: 222ACBZX00018000) being used with software version: v2.7.3.0, it was discovered that there was a defect that resulted in a difference between the set number of rotations and the actual number of rotations in a specific mode when the product was used with our company's M5 handpiece.

Moderate

FDADec 15, 2021Nationwide• Medtronic Xomed, Inc.

THERAKOS CELLEX Kit (Mallinckrodt) – Shipping Case Issue (2021)

This recall was initiated to recover a Dunnage Case, which is a case of three (3) CLXUSA kits. This Dunnage Case was shipped on 02-Dec-2021. Dunnage is used during the sterilization process and is not intended for customer use.

Low

FDADec 10, 2021Nationwide• Mallinckrodt Pharmaceuticals Ireland Ltd College Business & Technology Park Blanchardstown Road North Dublin

NaturesPlus Glucosamine (Ambix Laboratories) – Microbial Contamination (2021)

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCT: microbial contaminant identified as Pluralibacter gergoviae.

Class IIModerate

FDADec 6, 2021NY• Organics Corporation of America DBA Ambix Laboratories

ImagePilot Software (Konica Minolta) – Measurement Risk (2021)

lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel potential risk of incorrect length measurement/area calculation if incorrect power sequence is followed

Moderate

FDADec 3, 2021Nationwide• Konica Minolta Healthcare Americas, Inc.

Zenition 70 (Philips) – Foot Switch Failure (2021)

Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used or if the wired foot switch is not connected to the system.

Moderate

FDADec 2, 2021AZ, CA, FL +23 more• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Zenition 50 (Philips) – Foot Switch Failure (2021)

Moderate

FDADec 2, 2021AZ, CA, FL +23 more• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Veradius Unity (Philips) – Foot Switch Failure (2021)

Moderate

FDADec 2, 2021AZ, CA, FL +23 more• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Proteus 235 (Ion Beam) – Software Environment Risk (2021)

Proton Therapy System (PTS) software can be started in the clinical environment (clinical user) while some processes are still running in the test environment (tcs user). Initiating the startup of the clinical processes in the environment is not prevented even if some processes of the test environment (tcs) are still running. It may lead to situations where the system is using test processes without notifying the clinical user. If the versions of the processes are different between both environments, this could have an impact on patient treatments.

High

FDANov 29, 2021IN, NJ, OK +2 more• Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium

Wirion Embolic System (Cardiovascular Systems) – Filter Withdrawal Risk (2021)

Under certain circumstances, the WIRION filter assembly may become difficult to withdraw. Under such circumstances, alternative means may be necessary for withdrawal and the device may be prone to tearing or separating which may result in a risk for embolization.

FDANov 22, 2021Nationwide• Cardiovascular Systems Inc

Abre Venous Stent (Medtronic) – Migration Reports (2021)

There have been reports of stent migration.

FDANov 19, 2021Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Distractor Rack (Medtronic) – Gear Width Issue (2021)

Two lots of the 5598007 Distractor Rack which were not manufactured to specification. The crest width of the gear is too wide and may cause difficulty or the inability to operate the Distractor.

FDANov 19, 2021CT, IN, NE• Medtronic Sofamor Danek USA Inc

Pioneer and Talon ROVs (Honda) – crash and injury hazard (2021)

This recall involves the 2021 Honda Pioneer 700, Pioneer 1000, and Talon 1000 recreational off-highway vehicles (ROVs) equipped with electric power steering. The vehicles come in various colors including red, blue, green, gray, and yellow. "HONDA" is printed on the front, sides, and the rear of each vehicle. The name of the vehicle is printed on a label located on both sides of the vehicle. The VIN number is stamped in the frame at the left rear below the tilt-up bed/seat on the Pioneer 700 and Pioneer 1000. The VIN number is stamped in the frame on the left side under the left front fender for the Talon 1000. The VIN number range of affected vehicles for the Pioneer 700 is 1HFVE02**M4700031-M4700694, for the Pioneer 1000 is 1HFVE04**M4500061-M4502219, and for the Talon 1000 is 1HFVE05**M4200001-M4201598.

CPSCNov 18, 2021Nationwide• American Honda Motor Co. Inc., of Torrance, California

Evaporator Coil Drain Pans (Goodman) – installation risk (2021)

Fire/Burn Risk

This recall involves evaporator coil drain pans paired with residential condensing gas furnaces that are installed in a vertical, or "up-flow," configuration. Furnaces in this configuration that were installed or repaired with a new evaporator coil drain pan between January 2019 and November 2021 are affected by this recall. Only evaporator drain pans with serial numbers with prefixes ranging from 1901 through 2101 are covered by this recall. The evaporator coil, which sits atop the vertically installed furnace, will either be cased or uncased. The evaporator coil's serial number is displayed on a label attached to both cased and uncased models. For cased evaporator coils, the serial number is on the label attached to the coil case. For uncased units, the serial number is on a label attached to the front of the coil. It may be necessary to determine the brand and model number of your existing furnace in order to provide the correct repair kit. In most instances, the furnace brand and model number can be found on your furnace on the "Energy Guide" label. For all other instances, please refer to the instructions on Goodman's model verification tool at: www.recallrtr.com/drainpan The model number of the outdoor condenser your furnace is paired with may also be required. The model number can be found on a label attached to the outdoor condenser.

CPSCNov 18, 2021Nationwide• Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils)