Manufacturer
4 recalls in our database name H & L Jerch Sales, Inc. as the manufacturing or recalling firm.
Of the 4 recalls from H & L Jerch Sales, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
H & L Jerch Sales, Inc. is recalling Fertalin tablets because they contain synthetic equivalents of botanical constituents that have not been approved for use in dietary supplements.
H & L Jerch Sales, Inc. is recalling 1,981 bottles of Middle-Age Energy Booster tablets nationwide because they contain unapproved synthetic botanical ingredients.
H & L Jerch Sales, Inc. is recalling Eroxil tablets nationwide because they contain synthetic equivalents of spermine and/or spermidine, which are not approved for use in dietary supplements.
H & L Jerch Sales is recalling Erosyn tablets because they contain synthetic equivalents of botanical constituents that have not been approved for use in dietary supplements.