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McGuff Compounding Pharmacy Services, Inc.

McGuff Compounding Pharmacy Services, Inc. Recalls

All product recalls associated with McGuff Compounding Pharmacy Services, Inc..

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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 4721–4740 of 21320 recalls

Thiamine Hydrochloride Injection (McGuff) – Particulate Matter (2022)

Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.

Class IIModerate

FDADec 8, 2022Nationwide• McGuff Compounding Pharmacy Services, Inc.

Thiamine Hydrochloride 3000 mg (McGuff) – Foreign Substance (2022)

Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.

Class IIModerate

FDADec 8, 2022Nationwide• McGuff Compounding Pharmacy Services, Inc.

Trilogy 200 Ventilator (Philips) – Foam Separation (2022)

The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pressure and could cause the device to alarm.

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High

FDADec 7, 2022Nationwide• Philips Respironics, Inc.

Single-Use Packs (Johnson & Johnson) – Weld Protrusion (2022)

Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.

Moderate

FDADec 7, 2022FL, IL, MN +5 more• Johnson & Johnson Surgical Vision, Inc.

IMMULITE 2000 Thyroglobulin (Siemens) – Sensitivity Issue (2022)

Potential for Functional Sensitivity to not meet Instructions For Use (IFU) claims with the kit lots; control level one may result outside of published ranges; when control results are in range, users may observe increased imprecision with low level patient samples

Moderate

FDADec 7, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Quinapril Tablets 40mg (Lupin) – Impurity Limit Exceeded (2022)

CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

Class IIModerate

FDADec 7, 2022Nationwide• Lupin Pharmaceuticals Inc.

Quinapril Tablets 20mg (Lupin) – Impurity Limit Exceeded (2022)

CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

Class IIModerate

FDADec 7, 2022Nationwide• Lupin Pharmaceuticals Inc.

IMMULITE 2000 Thyroglobulin (Siemens) – Sensitivity Issue (2022)

Moderate

FDADec 7, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Lacosamide Oral Solution (Camber) – Excipient Specification Fail (2022)

Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content

Class IIILow

FDADec 6, 2022Nationwide• Camber Pharmaceuticals, Inc

STAT-IntraOp Immunoassay Kit (Future Diagnostics) – High Variability (2022)

Due to an issue of high coefficient of variability (CV) problem caused by the accuspheres inside the Immunoassay kits.

Moderate

FDADec 6, 2022AZ, CA, CO +4 more• Future Diagnostics Solutions B.V. Nieuweweg 279 Wijchen Netherlands

Surgical Container (Turbett Surgical) – Weld Failure (2022)

Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries.

High

FDADec 5, 2022Nationwide• Turbett Surgical, Inc.

Vanta Clinician Programmer (Medtronic) – Software Anomalies (2022)

Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"

Moderate

FDADec 3, 2022Nationwide• Medtronic Neuromodulation

Medical Cutting Needle (Remington) – Incorrect Stylet Length (2022)

The stylet is longer than specified on the label

Moderate

FDADec 2, 2022AL, CA, NC +3 more• Remington Medical, Inc.

Honda TRX90X ATVs (American Honda) - Crash Hazard (2022)

This recall involves model year 2022 Honda ATVs with model number TRX90X. The ATVs were sold in white and red. "HONDA" is printed on the front, sides, and rear of each vehicle. "TRX90X" is printed on a label located on both sides of the vehicle. The Vehicle Identification Number (VIN) is stamped on the front of the frame. The VIN range for the recalled vehicles are 1HFTE5505N4****** through 1HFTE5502N4******.

High

CPSCDec 1, 2022Nationwide• American Honda Motor Co. Inc., Torrance, California