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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

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 601–620 of 2399 recalls

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.

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

Sodium Chloride Injection (Fresenius) – Sterility Concern (2022)

Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.

1...29 303132 33...120

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Class IIModerate

FDANov 22, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

OttLite UVC Disinfecting Wand (Ottlite) – UV Radiation Excess (2022)

Product allows for the emission of ultraviolet (UV) electronic product radiation in excess of exposure limits recommended by the International Commission on Non-ionizing Radiation Protection (ICNIRP). The emissions are hazardous to users and others in the vicinity.

FDANov 17, 2022Nationwide• Ottlite TEchnologies, Inc.

Hass Avocados (Four Seasons) – Safety Concern (2022)

Sunrise Logistics Inc/ Four Seasons Produce Inc, 400 Wabash , Road Ephrata, PA 17522 has initiated a recall of, PROPAL Hass Avocados, Bag of 6 pieces, Green net with green plastic film, 11 bags per case because they were found to be contaminated with pesticides as per tolerance limit 40CFR 180.275.

Class IIILow

FDANov 15, 2022IN, NJ, PA• Four Seasons Produce Warehouse #2/Sunrise Logistics, Inc

NuVasive MAGEC Rod (NuVasive) – packaging sterility concern (2022)

During accelerated shelf-life extension studies it was noted that the final packaging was experiencing a potential of failure of the sterile packaging barrier which could result in a hazardous situation where the device is no longer sterile.

FDANov 1, 2022Nationwide• NuVasive Specialized Orthopedics, Inc.

Evolution MP Tibial Bases (MicroPort) – Incorrect Component (2022)

One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging.

FDAOct 28, 2022Nationwide• MicroPort Orthopedics Inc.

Cedar Creek Caramel Popcorn - gluten mislabeling (2022)

Label contains "Gluten Free" claim but product contains wheat and barley which are declared on the label.

Class IIModerate

FDAOct 27, 2022AZ, GA, IN +5 more• Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn

BD Nexiva IV Catheter (Becton Dickinson) – Shield Separation Risk (2022)

During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).

FDAOct 12, 2022FL, GA, IL +10 more• Becton Dickinson Infusion Therapy Systems Inc.

Sodium Chloride Injection (Fresenius) – Sterility Concern (2022)

Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.

Class IIModerate

FDAOct 11, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

NaturaLyte Liquid Acid (Fresenius) – Chemical Composition Error (2022)

The "Nominal Chemical Composition" section of the label incorrectly lists 5.62g/L KCL (potassium chloride). 5.62g/L actually corresponds to the CaCl (calcium chloride) content. The product remains potassium free.

FDAOct 4, 2022AL, AZ, CA +18 more• Fresenius Medical Care Holdings, Inc.

Zio AT Monitor (iRhythm) – ECG Notification Delay (2022)

Ambulatory ECG monitoring system labeling update: 1) Clinically actionable arrhythmia notifications delayed until patient registration is complete; 2) Patches limited to 100 symptomatic and 500 asymptomatic wireless transmissions; once the maximum transmission limit is reached for either type, any further transmissions for that type will cease. Risk of delayed reporting to health providers.

FDASep 28, 2022AL, AZ, AR +45 more• iRhythm Technologies, Inc.