Mckesson Aspirin Chewable Tablets Recall: Foreign Material Hazard
Mckesson Packaging Services recalls Aspirin Chewable Tablets (81mg) with foreign material in bulk inventory. Affected lots: 0113784, 0113786, 0113834, 0113887 (exp. 07/18).
Recall notice
Presence of Foreign Substance: foreign material found in the bulk inventory.
Contact the company
What happened, in plain English
Mckesson Packaging Services is recalling Aspirin Chewable Tablets (81mg) due to foreign material found in the bulk inventory. This could pose a risk if the foreign substance is ingested, though the specific hazard isn't detailed in the recall notice. Read more at govinfonow.com/recall/41864-mckesson-aspirin-chewable-tablets-recall-foreign-material-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/41864-mckesson-aspirin-chewable-tablets-recall-foreign-material-hazard · Updated October 8, 2026 · FDA enforcement record: FDA #D-0513-2017
Cite this page
“Mckesson Aspirin Chewable Tablets Recall: Foreign Material Hazard.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41864-mckesson-aspirin-chewable-tablets-recall-foreign-material-hazard. Based on FDA recall #D-0513-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0513-2017%22&limit=1).
Why it’s dangerous
The recall states that foreign material was found in the bulk inventory. This could potentially be ingested if the tablets are consumed, but the specific nature of the foreign substance and its potential harm are not described in the recall notice.
Who’s affected
People who purchased the Aspirin Chewable Tablets (81mg) from the listed lot numbers between July 2018 and the expiration date. Those who have the tablets in their possession are most at risk.
How to tell if you have this one
Check for lot numbers 0113784, 0113786, 0113834, or 0113887 on the packaging. The tablets expire July 2018 and are packaged in blisters per carton.
- Brand
Mckesson Packaging Services- Category
Drug
What to do — step by step
Check Product Lot Number
Look for lot numbers 0113784, 0113786, 0113834, or 0113887 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 20 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0513-2017 (February 23, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0513-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.