Pacific Healthcare, Inc dba B&B Pharmacy

Complete recall history across all FDA and CPSC categories — 16 total recalls

Pacific Healthcare, Inc dba B&B Pharmacy appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (16)

FDA drug safety enforcement actions by Pacific Healthcare, Inc dba B&B Pharmacy

Date Product Reason Class
Oct 7, 2015 Nandrolone 200 mg/ml Injection, 10 mL and 20 mL vials, Rx, B & B Health Mart ... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PGE1/PHENTO (30mg/50mcg/0.5mg/ml), Injection, 10 mL vial, Rx, B & B Heal... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PGE1/PHENTO (35mg/12mcg/1.5mg/ml), Injection, 10 mL vial, Rx, B & B Heal... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PGE1/PHENTO (30mg/40mcg/1mg/ml) Injection, 10 mL vial, Rx, B & B Health ... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PGE1/PHENTO (15mg/5mcg/0.5mg/ml) Injection, 5 mL and 10 mL vials, Rx, B ... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA+PGE1+PHENTO (30mg/20mcg/1mg/ml) Injection, 5 mL and 10 mL vials, Rx, B &... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 Stanozolol 200 mg/ml Injection, 20 mL vial, Rx, B & B Health Mart Pharmacy, B... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PGE1/PHENTO (22.5mg/8.33mcg/0.833mg/ml) Injection, 10 mL vial, Rx, B & B... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PGE 20mcg/ml Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflowe... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 Testosterone Cypionate 250 mg/mL Injection, 10 mL vial, Rx, B & B Health Mart... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 Testosterone prop. 200 mg/ml Injection, 10 mL vial, Rx, B & B Health Mart Pha... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PHENTO (15mg/0.8333mg/ml) Injection, 5 mL vial, Rx, B & B Health Mart Ph... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PHENTO (30mg/1mg/ml) Injection, 5 mL and 10 mL vials, Rx, B & B Health M... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PGE 25mcg/ml, Injection, 10 mL vial, Rx, B & B Health Mart Pharmacy, Bellflow... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PGE 30mcg/ml Injection, 10 mL vials, Rx, B & B Health Mart Pharmacy, Bellflow... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II
Oct 7, 2015 PAPA/PGE1/PHENTO (30mg/10mg/1mg/ml) Injection, 5 mL and 10 mL vials, Rx, B & ... Lack of Assurance of Sterility; FDA inspection identified GMP violations pote... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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