PlainRecalls
FDA Drug Verify with FDA Drug → Moderate Class II Terminated

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.

Reported: April 20, 2022 Initiated: April 4, 2022 #N/A 396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles units

Beak & Skiff Cider Mill, Inc. issued this FDA Drug recall on April 20, 2022. Classified as Moderate severity (Class II). Approximately 396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles units are affected. The recall was issued because: CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.. This recall notice is sourced from official FDA Drug enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

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 indicate 396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles units are affected, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.

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.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 4 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles

Related Recalls

6

0 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.

Details

Units Affected
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.
Location
La Fayette, NY

Recall Profile

Structured summary of the FDA Drug recall record
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.
Units affected 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.

Scale of Impact

396/12 oz. bottles, 11/5 gallon pails, 9/1 gallon jugs, 304/4 oz. bottles units affected — million-unit bracket.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units) ✓ This recall

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

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.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

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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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).