Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported April 20, 2022
BEAK & SKIFF SANITIZER Alcohol Antiseptic 80%, Topical Solution Antiseptic Hand Rub Non-Sterile Solution, Packaged in a) 12OZ/355ML bottles, UPC 48558 94603 6 b) 5 Gallon/18,927ML pail C)1 Gallon/3,785ML jug; d)4OZ/118ML spray top bottles; Produced By; Beak & Skiff Farms Apple Farms Inc. Lafayette, NY 13084.
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Beak & Skiff Cider Mill, Inc. recalled BEAK & SKIFF SANITIZER Alcohol Antiseptic 80%, Topical Solution Antiseptic Hand Rub Non-S… - a moderate-severity action.
BEAK & SKIFF SANITIZER Alcohol Antiseptic 80%, Topical Solution Antiseptic Hand Rub Non-S… was recalled by Beak & Skiff Cider Mill, Inc. in April 20, 2022. Reason: CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.. Check the official notice for the remedy. Verify recall #N/A with the FDA Drug before acting.
The recall
Beak & Skiff Cider Mill, Inc. issued this moderate-severity FDA Drug recall-CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits..
- Moderate
- severity level
- Class II
- classification
- April 20, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #N/A with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #N/A) was formally reported on April 20, 2022, with the manufacturer initiating the action on April 4, 2022. It is classified under Moderate severity (Class II), with a current status of Terminated. Beak & Skiff Cider Mill, Inc. is listed as the recalling firm, operating out of La Fayette, NY. Federal records list the affected scope as 396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles.
The documented reason for this recall is: CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits. Distribution data in the federal record shows the product reached: Distributed in NY and sales were made via the internet.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications 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
396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles
Related Recalls
6
5 from same agency
Product description
BEAK & SKIFF SANITIZER Alcohol Antiseptic 80%, Topical Solution Antiseptic Hand Rub Non-Sterile Solution, Packaged in a) 12OZ/355ML bottles, UPC 48558 94603 6 b) 5 Gallon/18,927ML pail C)1 Gallon/3,785ML jug; d)4OZ/118ML spray top bottles; Produced By; Beak & Skiff Farms Apple Farms Inc. Lafayette, NY 13084.
Reason for recall
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | N/A |
| Date reported | April 20, 2022 |
| Date initiated | April 4, 2022 |
| Recalling firm | Beak & Skiff Cider Mill, Inc. |
| Firm location | La Fayette, NY |
| Affected scope | 396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles |
| Distribution | Distributed in NY and sales were made via the internet. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (N/A) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug 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? ▼
BEAK & SKIFF SANITIZER Alcohol Antiseptic 80%, Topical Solution Antiseptic Hand Rub Non-Sterile Solution, Packaged in a) 12OZ/355ML bottles, UPC 48558 94603 6 b) 5 Gallon/18,927ML pail C)1 Gallon/3,785ML jug; d)4OZ/118ML spray top bottles; Produced By; Beak & Skiff Farms Apple Farms Inc. Lafayette, NY 13084.. Recalled by Beak & Skiff Cider Mill, Inc.. Units affected: 396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles.
Why was this product recalled? ▼
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 20, 2022. Severity: Moderate. Recall number: N/A.
Where was the recalled product distributed? ▼
Distribution: Distributed in NY and sales were made via the internet..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (N/A) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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: FDA Drug, reported April 20, 2022. 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.