PlainRecalls
CPSC Moderate Active

Desert Harvest Recalls Reléveum Skin Repair Cream Due to Failure to Meet Child Resistant Closure Requirements

Reported: September 25, 2018 Initiated: September 25, 2018 #18229

Product Description

The recalled Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle with a white pump dispenser cap and a tan/white gradient label with "Desert Harvest Reléveum" printed on the front. The product is an over the counter skin cream with lidocaine (4%) as the active ingredient. The cream is sold in a 4 ounce or an 8 ounce bottle with the date code "D02N5" printed above the barcode on the bottle.

Reason for Recall

The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if the contents are swallowed by young children.

Remedy

Consumers should immediately place the recalled pain relieving cream out of the reach of children and contact Desert Harvest for a free replacement child resistant cap for the bottle.

Details

Units Affected
About 1,450
Official Source
https://www.cpsc.gov/Recalls/2018/Desert-Harvest-Recalls-Releveum-Skin-Repair-Cream-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirements

Frequently Asked Questions

What product was recalled? ▼
The recalled Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle with a white pump dispenser cap and a tan/white gradient label with "Desert Harvest Reléveum" printed on the front. The product is an over the counter skin cream with lidocaine (4%) as the active ingredient. The cream is sold in a 4 ounce or an 8 ounce bottle with the date code "D02N5" printed above the barcode on the bottle.. Recalled by Desert Harvest Inc., of Hillsborough, N.C.. Units affected: About 1,450.
Why was this product recalled? ▼
The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if the contents are swallowed by young children.
What should consumers do? ▼
Consumers should immediately place the recalled pain relieving cream out of the reach of children and contact Desert Harvest for a free replacement child resistant cap for the bottle.
Which agency issued this recall? ▼
This recall was issued by the CPSC on September 25, 2018. Severity: Moderate. Recall number: 18229.

Related Recalls

FDA Devices Moderate

Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…

Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…

Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate

Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…

Fujirebio Diagnostics, Inc. · 2026-02-11

Explore Related Data

Vehicle Safety → Drug Information →