Ridge Properties recalls

Ridge Properties has 11 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 25 Sep 2019. The most frequent reason is processing deviation.

Total recalls11since 2017

Last 12 months0reported

Class I00% of total

Ongoing0latest 25 Sep 2019

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 11 100%Class III 0 0%

Why ridge properties is recalled

Product types

Pain Medication11100%

By year

2019655%
2017545%

All ridge properties recalls, newest first

11 total

Reported	Class	Recall	Company	Reason	Where
25 Sep 2019Drug	CLASS II	Superior Pain & Itch Relief (lidocaine) Cream recalled	Ridge Properties	Potency & Assay	Nationwide
25 Sep 2019Drug	CLASS II	Soothing Sore Relief (lidocaine) Cream recalled by Ridge Properties	Ridge Properties	Potency & Assay	Nationwide
25 Sep 2019Drug	CLASS II	Soothing Sore Relief (lidocaine) Liquid Gel recalled by Ridge Properties	Ridge Properties	Potency & Assay	Nationwide
25 Sep 2019Drug	CLASS II	Pre-tat (lidocaine) 1 Pre Tattoo Prep With Lidocaine Cream recalled	Ridge Properties	Sterility	Nationwide
25 Sep 2019Drug	CLASS II	Superior Pain & Itch Relief (lidocaine) Liquid Gel recalled	Ridge Properties	Potency & Assay	Nationwide
25 Sep 2019Drug	CLASS II	Pre-tat (lidocaine) 1 Pre Tattoo Prep With Lidocaine Liquid Gel recalled	Ridge Properties	Sterility	Nationwide
29 Nov 2017Drug	CLASS II	Extra Strength Naturally HL Hemorrhoid Numbing Spray recalled	Ridge Properties	Processing Deviation	OR
29 Nov 2017Drug	CLASS II	Extra Strength PreTAT by TAT BALM Gel, (lidocaine HCL 4%) Gel recalled	Ridge Properties	Processing Deviation	OR
29 Nov 2017Drug	CLASS II	Extra Strength Naturally HL Hemorrhoid Numbing recalled	Ridge Properties	Processing Deviation	OR
29 Nov 2017Drug	CLASS II	Extra Strength Naturally HL Bed Sore Relief Cream recalled	Ridge Properties	Processing Deviation	OR

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.