Gustav Selter GmbH Co. & KG, of Germany recalls
1 recall recorded since 2018, most recently on 6 November 2019. Status and classification are as published by the CPSC.
Recalls1
Ongoing (FDA)0
Terminated or completed0
Class I (FDA)0
Announced Consumer products
- Recall started
- 6 November 2019
- Reason
- The shaft of the knitting needle can split or burst, posing a laceration hazard.
- Remedy
- Consumers should immediately stop using the recalled knitting needles and contact the store where purchased for a full refund in the form of a store voucher.
- Recall number
- 20017
- US 6 (4.0mm) addi® FlipStix knitting needles
CPSC recall notice
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.