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Class III: unlikely to cause harmTerminated

ITW Dymon Lemon Hand Sanitizing Wipes [n-alkyl Recall

Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride (0

ITW Dymon · Olathe, KS

Risk level
Class III
Reported by FDA
Nov 21, 2012
Recall ID
D-056-2013
Check your lot numberHow we source this data

Summary

ITW Dymon recalled Lemon Hand Sanitizing Wipes [n-alkyl starting Sep 28, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-056-2013 on Nov 21, 2012. Reason: CGMP Deviations: The products were manufactured with raw material which contain unknown particles believed to be water and dirt. Status: Terminated.

Why it was recalled

CGMP Deviations: The products were manufactured with raw material which contain unknown particles believed to be water and dirt.

Product description

Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride (0.1%) and n-alkyl dimethyl ethyl benzyl ammonium chloride (0.1%)], labeled as a) Genuine Joe Cleaning Supplies, Lemon Scent, Anti-microbial Hand Sanitizing Wipes, 120-count premoistened wipes per bucket, 6 buckets per case, Manufactured for S.P. Richards Co., 6300 Highlands Pkwy., Smyma, GA 30082, UPC 0 35255 10477 7; b) Pro Chem Lemon Aid, Hand Sanitizing Wipes, 85-count premoistened wipes per bucket, 6 buckets per case, An exclusive product of: Pro Chem, Inc., 1475 Bluegrass Lakes Parkway, Alpharetta, GA 30004; c) Scrubs, Lemon Hand Sanitizer Wipes, 120-count premoistened wipes per bucket, 6 buckets per case, Manufactured in the U.S.A. by ITW Dymon, 805 E. Old 56 Highway, Olathe, KS 66061, UPC 7 64769 92991 9.

Lot numbers, UPCs & expiration codes

Lot #: a) B26221, Exp 09/18/15; b) B94221, Exp 09/05/15; c) B94221, Exp 09/05/15

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-056-2013
Classification
Class III
Status
Terminated
Recall initiated
Sep 28, 2012
FDA report date
Nov 21, 2012
Quantity
a) 216 cases; b) 75 cases; c) 29 cases
Recall type
Voluntary: Firm initiated
Recalling firm
ITW Dymon

Original FDA data

Every field from FDA enforcement report D-056-2013, exactly as published.

Show all FDA fields
City
Olathe
State
KS
Status
Terminated
Country
United States
Event ID
63428
Address
805 E Old 56 Hwy
Code information
Lot #: a) B26221, Exp 09/18/15; b) B94221, Exp 09/05/15; c) B94221, Exp 09/05/15
Postal code
66061
Report date
Nov 21, 2012
Product type
Drugs
Recall number
D-056-2013
Classification
Class III
Recalling firm
ITW Dymon
Product quantity
a) 216 cases; b) 75 cases; c) 29 cases
Termination date
Mar 25, 2014
Reason for recall
CGMP Deviations: The products were manufactured with raw material which contain unknown particles believed to be water and dirt.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride (0.1%) and n-alkyl dimethyl ethyl benzyl ammonium chloride (0.1%)], labeled as a) Genuine Joe Cleaning Supplies, Lemon Scent, Anti-microbial Hand Sanitizing Wipes, 120-count premoistened wipes per bucket, 6 buckets per case, Manufactured for S.P. Richards Co., 6300 Highlands Pkwy., Smyma, GA 30082, UPC 0 35255 10477 7; b) Pro Chem Lemon Aid, Hand Sanitizing Wipes, 85-count premoistened wipes per bucket, 6 buckets per case, An exclusive product of: Pro Chem, Inc., 1475 Bluegrass Lakes Parkway, Alpharetta, GA 30004; c) Scrubs, Lemon Hand Sanitizer Wipes, 120-count premoistened wipes per bucket, 6 buckets per case, Manufactured in the U.S.A. by ITW Dymon, 805 E. Old 56 Highway, Olathe, KS 66061, UPC 7 64769 92991 9.
Distribution pattern
Nationwide
Recall initiation date
Sep 28, 2012
Initial firm notification
Telephone
Center classification date
Nov 15, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-056-2013, published Nov 21, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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