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Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Vita Pharmacy, LLC dba Talon Compounding Pharmacy Recalls

All product recalls associated with Vita Pharmacy, LLC dba Talon Compounding Pharmacy.

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Recall Summary

Total Recalls

1000

Past Year

567

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 2441–2460 of 7756 recalls

Alprostadil 32mcg Injection (Talon) – sterility concern (2021)

Lack of assurance of sterility

Class IIModerate

FDAOct 12, 2021Nationwide• Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Testosterone Bi-Blend (Talon) – sterility risk (2021)

Lack of assurance of sterility

Class IIModerate

FDAOct 12, 2021Nationwide• Vita Pharmacy, LLC dba Talon Compounding Pharmacy

Clark Laboratories, Inc.: Bartels Legionella Urinary Antigen- an adjunct to culture...

Contamination of the conjugate may cause a pipetting issue which then could lead to an invalid assay

1...121 122123124 125...388

Page 123 of 388Next

FDA

Oct 11, 2021

OH, UT

• Clark Laboratories, Inc.

Jjgc Industria E Comercio De Materials Dentarios Sa Av Juscelino Kubitschek De Oliveira Curitiba Brazil: GM Helix Acqua Implant 3.5x10, Article No. 140.944

3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline cases where the bone quality is low and the bone ridge has a maximum indication for the implant height (10mm), if the incorrect implant is installed, it could result in damage to the nerve or adjacent bone structures/cavities.

FDAOct 11, 2021Nationwide• Jjgc Industria E Comercio De Materials Dentarios Sa Av Juscelino Kubitschek De Oliveira Curitiba Brazil

BioFire Diagnostics, LLC: BioFire Blood Culture Identification 2 (BCID2) Panel Part...

Due to an increased risk of false positive Acinetobacter calcoaceticus- baumannii complex results. The cause may be as a due to non-viable contamination in the blood culture vials.

FDAOct 11, 2021Nationwide• BioFire Diagnostics, LLC

Beaver Visitec International, Inc.: bvi CustomEyes Kit-Lafayette General Medical Center: Cust...

Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades

FDAOct 8, 2021Nationwide• Beaver Visitec International, Inc.

Beaver Visitec International, Inc.: bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that...

Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades

FDAOct 8, 2021Nationwide• Beaver Visitec International, Inc.

Beaver Visitec International, Inc.: Beaver Xstar Crescent Knife, 2.5mm, 55 degrees, bevel dow...

Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades

FDAOct 8, 2021Nationwide• Beaver Visitec International, Inc.

Beaver Visitec International, Inc.: bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wa...

Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades

FDAOct 8, 2021Nationwide• Beaver Visitec International, Inc.

SCIENCE & BIO MATERIALS Zi Du Monge Lourdes France: ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605

Mislabeled product.

FDAOct 7, 2021Nationwide• SCIENCE & BIO MATERIALS Zi Du Monge Lourdes France

Primus Corporation dba Trinity Biotech: Trinity Biotech HbA1c (GHb) Contorls Kit, 500uL (Levels I...

The Control Level I material value was showing results exceeding the upper limit of the acceptable range after a period of three (3) months. Additionally, per the firm, the unacceptable Control Level 1 value results in the Analyzer generating an error code which stops further testing and nullifies associated patient samples, resulting in a delay in patient results and a potential delay in therapeutic modifications.

FDAOct 5, 2021Nationwide• Primus Corporation dba Trinity Biotech

Primus Corporation dba Trinity Biotech: A. MENARINI diagnostics Hb 9210 PREMIER, LEVEL1, LEVEL II...

The Control Level I material value was showing results exceeding the upper limit of the acceptable range after a period of three (3) months. The unacceptable Control Level 1 value results in the Analyzer generating an error code which stops further testing and nullifies associated patient samples, resulting in a delay in patient results and a potential delay in therapeutic modifications.

FDAOct 5, 2021Nationwide• Primus Corporation dba Trinity Biotech

Omeprazole Capsules (Dr. Reddy's) – Foreign Object Risk (2021)

CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.

Class IIModerate

FDAOct 5, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Ezetimibe Simvastatin 10/40mg (Dr. Reddy's) – Excipient Specifications (2021)

Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity

Class IIModerate

FDAOct 5, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Ezetimibe Simvastatin 10/20mg (Dr. Reddy's) – Excipient Specifications (2021)

Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity

Class IIModerate

FDAOct 5, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Ezetimibe Simvastatin 10/80mg (Dr. Reddy's) – Excipient Specifications (2021)

Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity

Class IIModerate

FDAOct 5, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Ezetimibe Simvastatin 10/40mg (Dr. Reddy's) – Excipient Contamination (2021)

Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle

Class IIModerate

FDAOct 5, 2021Nationwide• Dr. Reddy's Laboratories, Inc.