Severity
Moderate
ModerateActive
CPSC recall · Reported November 6, 2019
Skacel Collection Recalls FlipStix Knitting Needles Due to Laceration Hazard
The shaft of the knitting needle can split or burst, posing a laceration hazard.
Compiled from official public sources by the editorial team.
Verify with CPSC →
Gustav Selter GmbH Co. & Kg, of Germany recalled This recall involves US 6 (4.0mm diameter) FlipStix in 6" and 8" long knitting needles. T… - a moderate-severity action.
Skacel Collection Recalls FlipStix Knitting Needles Due to Laceration Hazard was recalled by Gustav Selter GmbH Co. & Kg, of Germany in November 6, 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 sto…. Verify recall #20017 with the CPSC before acting.
The recall
Gustav Selter GmbH Co. & Kg, of Germany issued this moderate-severity CPSC recall-The shaft of the knitting needle can split or burst, posing a laceration hazard..
- Moderate
- severity level
- November 6, 2019
- reported
Sourced from official CPSC enforcement records. Verify recall #20017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #20017) was formally reported on November 6, 2019. It is classified under Moderate severity, with a current status of Active. Gustav Selter GmbH Co. & Kg, of Germany is listed as the recalling firm. Federal records list the affected scope as About 270.
The documented reason for this recall is: The shaft of the knitting needle can split or burst, posing a laceration hazard. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: 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. - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 3 from CPSC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 270
Related Recalls
6
3 from same agency
Product description
This recall involves US 6 (4.0mm diameter) FlipStix in 6" and 8" long knitting needles. The knitting needles have aluminum shafts that are tapered at both ends. The long shaft holds the active (unsecured) stitches of the fabric, to prevent them from unravelling, whereas the tapered ends are used to form new stitches. The knitting needles were sold in blue, red and yellow combination packages. There are five needles per pack.
Reason for recall
The shaft of the knitting needle can split or burst, posing a laceration hazard.
Remedy, what to do
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 Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 20017 |
| Date reported | November 6, 2019 |
| Date initiated | November 6, 2019 |
| Recalling firm | Gustav Selter GmbH Co. & Kg, of Germany |
| Affected scope | About 270 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately stop using the recalled knitting needles and contact the store where purchased for a full refund in …
- Check the recall number (20017) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
This recall involves US 6 (4.0mm diameter) FlipStix in 6" and 8" long knitting needles. The knitting needles have aluminum shafts that are tapered at both ends. The long shaft holds the active (unsecured) stitches of the fabric, to prevent them from unravelling, whereas the tapered ends are used to form new stitches. The knitting needles were sold in blue, red and yellow combination packages. There are five needles per pack.. Recalled by Gustav Selter GmbH Co. & Kg, of Germany. Units affected: About 270.
Why was this product recalled? ▼
The shaft of the knitting needle can split or burst, posing a laceration hazard.
What should consumers do? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the CPSC on November 6, 2019. Severity: Moderate. Recall number: 20017.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (20017) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported November 6, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.