Recall Register

Pharmatech LLC: FDA recalls

FDA enforcement reports name Pharmatech LLC as the recalling firm in 5 events. The events have 53 product records. The recalls started from 2015 to 2017.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

5 events, newest first.

FDA enforcement events of Pharmatech LLC
InitiatedProduct (first record)TypeClassRecordsStatus
16 Aug 2017Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85, Manufactured by PharmaTech LLC, Davie, FLDrugClass II4Terminated
16 Aug 2017Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-0160-97FoodClass II17Terminated
8 Aug 2016Sennazon (sennosides) Syrup, 8.8 mg, 8 fl. oz. (237 mL) bottle, Mfd. for: Bayshore Pharmaceuticals, Tampla, FL 33619, NDC 76518-100-08.DrugClass II7Terminated
8 Aug 2016Virtrate-2, Sodium Citrate-Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.FoodClass II23Terminated
9 Mar 2015Rugby Poly Vitamin Liquid, 50mlFoodClass II2Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Pharmatech LLC: events for each product type
TypeEvents
Food3
Drug2
Pharmatech LLC: events in each class
ClassEvents
Class II5
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
0

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Pharmatech LLC, by the year that the recall started. The largest year is 2016, with 2 events.

Official channels

Cite this page

Recall Register. Pharmatech LLC: FDA recalls. https://recallregister.com/firm/pharmatech-llc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
FL

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Pharmatech LLC have?
Class II: 5 events. The class is for the product of a recall. It is not a class of the firm.
Which product types do the FDA recalls of Pharmatech LLC have?
Food: 3 events. Drug: 2 events.
What is the newest FDA recall of Pharmatech LLC?
FDA event 77960, which the firm started on 16 Aug 2017. The first product in the record is: Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85, Manufactured by PharmaTech LLC, Davie, FL
How many FDA recalls of Pharmatech LLC have the status Ongoing?
No event has the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.