Recall Register

Food, drugs, devices › Firms

Paddock Laboratories, LLC.

FDA recalling firm · 3 enforcement events · 3 product records · 2012–2018 · MN

Paddock Laboratories, LLC. has 3 FDA enforcement events on this register (3 product records) between 2012 and 2018: 3 drug; the busiest year was 2012 with 1.

0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in MN.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
26 Feb 2018Evamist (estradiol transdermal spray), 1.53mg estradiol/spray, 0.27 fl oz (8.1 mL) per bottle, Rx Only, Manufactured for Perrigo, Minneapolis, MN 55427. NDC: 0574-2067-27DrugClass II1Terminated
11 Mar 2014Perrigo, Clindamycin Palmitate Hydrochloride for Oral Solution, USP, 75mg/5mL, 100 ml, NDC 0574-0129-01DrugClass II1Terminated
3 Oct 2012Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,DrugClass II1Terminated

By type and class

Drug3
Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

12
14
16
18
20
22
24
26
Enforcement events for Paddock Laboratories, LLC. by year initiated.

Questions and answers

How many FDA recalls has Paddock Laboratories, LLC. had?

3 enforcement events (3 product records) on this register, 2012–2018: 3 drug.

Are any Paddock Laboratories, LLC. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Paddock Laboratories, LLC. recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.