North American Custom Laboratories recalls

North American Custom Laboratories has 7 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 27 Apr 2022. The most frequent reason is sterility.

Total recalls7since 2022

Last 12 months0reported

Class I00% of total

Ongoing0latest 27 Apr 2022

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 7 100%Class III 0 0%

Why north american custom laboratories is recalled

Sterility7100%

Product types

Injectable & IV Drugs7100%

By year

20227100%

All north american custom laboratories recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
27 Apr 2022Drug	CLASS II	LL-37 2 mg/mL Injection vials recalled by North American Custom	North American Custom Laboratories	Sterility	Nationwide
27 Apr 2022Drug	CLASS II	BPC-157 2 mg/mL Injection vials recalled by North American Custom	North American Custom Laboratories	Sterility	Nationwide
27 Apr 2022Drug	CLASS II	Sermorelin Acetate 1 mg/mL Injection vials recalled	North American Custom Laboratories	Sterility	Nationwide
27 Apr 2022Drug	CLASS II	Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL Injection vials recalled	North American Custom Laboratories	Sterility	Nationwide
27 Apr 2022Drug	CLASS II	Melanotan II 1 mg/mL Injection vials recalled by North American Custom	North American Custom Laboratories	Sterility	Nationwide
27 Apr 2022Drug	CLASS II	ARA-290 (Cibinetide Acetate) 6 mg/mL Injection vials recalled	North American Custom Laboratories	Sterility	Nationwide
27 Apr 2022Drug	CLASS II	PT-141 (Bremelanotide Acetate) 10 mg/mL Injection vials recalled	North American Custom Laboratories	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.