Primark Recalls Kitten Heel Court Shoes Due to High Levels of Chromium; Risk of Skin Irritation
Reported: May 27, 2020 Initiated: May 27, 2020 #20127
Product Description
This recall involves the Primark Wide Fit Kitten Heel Court Shoes. The pumps have an approximately 1.5 inch heel. The shoes were sold in black and nude microfiber fabric. Product number 06689 and the RN code 145478 are printed on the inside of the shoe.
Reason for Recall
The leather insock in the shoes has elevated levels of Chromium VI, posing a risk of skin irritation.
Remedy
Consumers should immediately stop using the recalled shoes and return the shoes to a Primark store for a full refund of the purchase price.
Details
- Units Affected
- About 1,700
Frequently Asked Questions
What product was recalled? ▼
This recall involves the Primark Wide Fit Kitten Heel Court Shoes. The pumps have an approximately 1.5 inch heel. The shoes were sold in black and nude microfiber fabric. Product number 06689 and the RN code 145478 are printed on the inside of the shoe.. Units affected: About 1,700.
Why was this product recalled? ▼
The leather insock in the shoes has elevated levels of Chromium VI, posing a risk of skin irritation.
What should consumers do? ▼
Consumers should immediately stop using the recalled shoes and return the shoes to a Primark store for a full refund of the purchase price.
Which agency issued this recall? ▼
This recall was issued by the CPSC on May 27, 2020. Severity: Moderate. Recall number: 20127.
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