Asteria Health Recalls Estradiol Pellets Over Metal Contamination Risk
Asteria Health recalled 14,848 estradiol pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The recall is classified as Class II, indicating a high hazard level.
Quick Facts at a Glance
Recall Date
January 26, 2026
Hazard Level
HIGH
Brand
F.H. INVESTMENTS, Inc.
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL
Hazard Information
Presence of Foreign substance - potential presence of metal particulate matter
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact F.H. INVESTMENTS, Inc. (dba Asteria Health) or your healthcare provider for guidance. Notification method: Letter
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
No spamUnsubscribe anytime
Product Details
The recalled product is ESTRADIOL, 15 mg, 1 Sterile Pellet, with NDC: 79559-3015-32. It was distributed nationwide in the USA. The affected lot numbers include 253000118, 253000145, 253000146, and 253000167, with expiration dates ranging from June 30, 2026, to September 23, 2026.
The Hazard
The recall was initiated due to the potential presence of metal particulate matter in the pellets. This contamination can pose serious health risks if ingested.
Reported Incidents
As of the report date, no specific incidents or injuries have been documented related to this recall. However, the potential health risks associated with metal contamination remain significant.
What to Do
Consumers should stop using the estradiol pellets immediately. Contact F.H. Investments, Inc. (dba Asteria Health) or your healthcare provider for further guidance and potential refund options.
Contact Information
For more information, consumers can contact F.H. Investments, Inc. at their Birmingham, AL office. Additional details can be found at the FDA recall page: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0310-2026.
Taro Pharmaceuticals announced a market withdrawal of Diclofenac Sodium, Topical Gel, 3% on January 27, 2026. The withdrawal stems from out of specification viscosity results. Healthcare providers and consumers should stop using the product immediately.
Fresenius Kabi Compounding recalled 1,057 bags of Acyclovir Sodium Injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers should cease use immediately and contact the manufacturer for guidance.
Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.
Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.
Fresenius Kabi Compounding recalled 1,410 bags of ketamine HCl injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers and consumers must stop using this product immediately.
Fresenius Kabi Compounding recalled 10,548 bags of thiamine HCl injection on February 5, 2026. The recall follows a lack of assurance of sterility, posing a high health risk. Affected products include several lots expiring between February and May 2026.
Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.
Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.