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Microbiologics Inc

Microbiologics Inc Recalls

All product recalls associated with Microbiologics 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 5061–5080 of 21320 recalls

Helix Elite Inactivated Standard (Microbiologics) – UK Registration (2022)

Product not registered for use in the UK

Moderate

FDAJul 27, 2022Nationwide• Microbiologics Inc

Orca Foam Cube (Gelita Medical) – Endotoxin Levels (2022)

In routine bioburden testing, higher than acceptable levels of Endotoxins were observed.

Moderate

FDAJul 27, 2022Nationwide• GELITA MEDICAL GMBH Uferstr. 7 Eberbach Germany

Divalproex Sodium Tablets (Amneal) – Dissolution Failure (2022)

Failed dissolution specifications.

Class IIModerate

FDAJul 27, 2022

1...252 253254255 256...1066

Page 254 of 1066Next

Nationwide

• Amneal Pharmaceuticals of New York, LLC

Bupivacaine Lidocaine Solution (Pine) – Sterility Issue (2022)

Lack of Assurance of Sterility

Class IIModerate

FDAJul 27, 2022AL, CA, IN +2 more• Pine Pharmaceuticals, LLC

Azacitidine Injection (Amerisource) – Subpotent Drug (2022)

Subpotent Drug

Class IIILow

FDAJul 27, 2022Nationwide• Amerisource Health Services LLC

Vanta Clinician Programmer (Medtronic) – Communication Issue (2022)

Potential communication issue in which the Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 may be unable to connect with a Vanta Implantable Neurostimulator (INS) Model 977006 when a patient is implanted with more than one neurostimulator.

Moderate

FDAJul 26, 2022AL, AK, AZ +47 more• Medtronic Neuromodulation

Vanta Clinician Programmer (Medtronic) – Error Code Issue (2022)

Potential for Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 to display an Unexpected Device Error Code 1502 Message, and the user will be unable to perform programming of the Vanta Implantable Neurostimulator (INS) Model 977006.

Moderate

FDAJul 26, 2022Nationwide• Medtronic Neuromodulation

NARMD Medical Depot Forceps (Stradis) – Sterile Barrier (2022)

The sterile barrier may be compromised.

Low

FDAJul 25, 2022Nationwide• Stradis Medical, LLC dba Stradis Healthcare

NARMD Medical Depot Scissors (Stradis) – Sterile Barrier (2022)

The sterile barrier may be compromised.

Low

FDAJul 25, 2022Nationwide• Stradis Medical, LLC dba Stradis Healthcare

Pantoprazole Sodium Suspension (Sun Pharmaceutical) – Discoloration (2022)

Discoloration

Class IIModerate

FDAJul 25, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

HLS Set Advanced (Maquet) – Sterility Barrier (2022)

The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated November 6, 2020).

Moderate

FDAJul 22, 2022Nationwide• Maquet Medical Systems USA

HLS Set Advanced (Maquet) – Sterility Barrier (2022)

Moderate

FDAJul 22, 2022Nationwide• Maquet Medical Systems USA

Azacitidine Injection (Teva) – Subpotent Medication (2022)

Subpotent Drug - Out of specification (OOS) result obtained during monitoring stability study for Assay. Results below specification.

Class IIILow

FDAJul 22, 2022IN, OH• Teva Pharmaceuticals USA Inc

Autosoft 90 Cannula (Unomedical) – Insulin Fill Value (2022)

The IFU incorrectly states the insulin fill value of two sizes of cannula which can result in an initial insulin infusion to be fewer units than intended.

Low

FDAJul 21, 2022CA• Unomedical A/S Aaholmvej

Matzim LA (Teva) – Dissolution Specification Failure (2022)

Failed Dissolution Specifications: below specification limits for dissolution.

Class IIModerate

FDAJul 21, 2022Nationwide• Teva Pharmaceuticals USA Inc

Matzim LA Tablets (Teva) – Dissolution Failure (2022)

Failed Dissolution Specifications: below specification limits for dissolution.

Class IIModerate

FDAJul 21, 2022Nationwide• Teva Pharmaceuticals USA Inc

PICS Ground Cinnamon (International Spice) – Mislabeled Product (2022)

Cumin mislabeled as cinnamon

Class IIILow

FDAJul 21, 2022IN, MA• Gourmet Spice LLC dba International Spice

iSED Primary Pump Tubing (Alcor Scientific) – Biohazard Leak Risk (2022)

Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto an ALCOR iSED ESR Analyzer, there is a potential of a biohazard leak from the iSEDs Probe Tube

High

FDAJul 20, 2022Nationwide• Alcor Scientific, Inc.

VITROS XT 7600 System (Ortho-Clinical) – Electrical Current Shift (2022)

Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems may cause a positive or negative shift in the electrical current supplied to the LED used in conjunction with the Digital Imaging Reflectometer. Potential exists for either a positive or negative shift in results reported by the VITROS System.

Moderate

FDAJul 19, 2022Nationwide• Ortho-Clinical Diagnostics, Inc.

VITROS XT 3400 System (Ortho-Clinical) – Electrical Current Shift (2022)

Moderate

FDAJul 19, 2022Nationwide• Ortho-Clinical Diagnostics, Inc.