CLASS III Food recall · Reported 24 Apr 2024 · FDA Enforcement Report
Windsor Black Peppercorns grinder recalled by Morton Salt
Morton Salt is recalling Windsor Black Peppercorns grinder. The recall was initiated on 29 Mar 2024 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1149-2024
- FDA event ID
- 94344
- Recalling firm
- Morton Salt, Chicago, IL
- Brand
- Windsor
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 29 Mar 2024
- FDA classified
- 12 Apr 2024
- Reported
- 24 Apr 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Product category
- Other
Timeline
| 29 Mar 2024 | Recall initiated by company | |
| 12 Apr 2024 | Classified by FDA | +14 days |
| 24 Apr 2024 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Label mix-up product is labeled as black peppercorn but is actually Pink Himalayan salt
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Windsor Black Peppercorns, 34g grinder, UPC 0 66010 08200 9, 6 units per wholesale case
Where it was distributed
Canada
Questions about this recall
Is Windsor Black Peppercorns grinder recalled?
Yes. Morton Salt recalled Windsor Black Peppercorns grinder on 29 Mar 2024. The recall is Class III and its status is Terminated. Recall number F-1149-2024.
Why was it recalled?
Label mix-up product is labeled as black peppercorn but is actually Pink Himalayan salt
Which lots are affected?
lot code, ZX23060001
Where was it sold?
Canada
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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