Pepsico Inc FDA Inspection Record

FEI 3003014383 · Inspections, Form 483s, warning letters and import refusals

Pepsico Inc is an FDA-inspected facility (FEI 3003014383) located in Purchase, NY, US. RegDataLab tracks 2 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 25, 2025: No Action Indicated (NAI)
Inspections on record
2 (2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
15, latest Sep 25, 2026

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Mar 25, 2025No Action Indicated (NAI)No citations listed
Nov 1, 2018No Action Indicated (NAI)No citations listed

Recalls

Showing the 10 most recent of 15 recalls. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Sep 25, 2026Class IIH-0009-202728 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange…
Undeclared Yellow No. 6 and/or Yellow No. 5
Sep 17, 2025Class IIH-0010-2026Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as…
Undeclared sugar in finished product-primary package does not reflect the product inside bottle.
Mar 9, 2024Class IIF-1120-2024Schweppes ZERO SUGAR GINGER ALE CAFFIENE FREE 7.5 FL OZ (221 mL) PRODUCED UNDER THE…
During an internal investigation the firm discovered that product labeled as Zero Sugar contains full sugar product.
Oct 27, 2023Class IIF-0314-2024Crush Orange Soda, 24 Pack. 24 - 12 oz. cans. Caffeine Free. Contains No Juice. UPC 0…
foreign material - plastic
Jul 8, 2023Class IIIF-1286-2023Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles. UPC # 0-12000-01722-3
Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)
Jan 28, 2023Class IIF-0352-2023Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 Fl Oz (405mL). UPC 0…
Foreign object (glass).
Aug 17, 2022Class IIIF-1738-2022Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as 12 pack. Bottled under the…
The outer wraps match the liquid in the can (Zero Sugar - Mountain Dew Major Melon) however the primary package (can) is incorrect (Full…
Aug 15, 2022Class IIF-1724-2022Starbucks Vanilla Espresso Triple Shot, 15 oz, 12 bottles per case.
Possible contamination by foreign material (metal fragments).
Apr 2, 2022Class IIF-0982-2022Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ Bottles. UPC on retail 24…
Immediate package (individual 16.9 FL OZ bottle) is incorrectly labeled as the zero sugar variety, the product inside the bottle is the…
Sep 26, 2021Class IIF-0089-2022Starbucks Doubleshot Espresso, Espresso & Cream, 6.5 FL OZ UPC 012000001772 and 2 more products
An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.

FDA record score

23 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

10 records behind this number
RecordDatePoints x age weightAdds
Class II recall H-0009-2027, this FEI as the recalling firmSep 25, 20264 x 14
Class II recall H-0010-2026, this FEI as the recalling firmSep 17, 20254 x 14
Class II recall F-1120-2024, this FEI as the recalling firmMar 9, 20244 x 0.62.4
Class II recall F-0314-2024, this FEI as the recalling firmOct 27, 20234 x 0.62.4
Class II recall F-0352-2023, this FEI as the recalling firmJan 28, 20234 x 0.62.4
Class II recall F-1724-2022, this FEI as the recalling firmAug 15, 20224 x 0.62.4
Class II recall F-0982-2022, this FEI as the recalling firmApr 2, 20224 x 0.62.4
Class II recall F-0089-2022, this FEI as the recalling firmSep 26, 20214 x 0.251
Class II recall F-0537-2021, this FEI as the recalling firmApr 29, 20214 x 0.251
Class II recall F-2091-2019, this FEI as the recalling firmAug 16, 20194 x 0.251

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Pepsico Inc
Location
Purchase, NY (US)
Source
inspections

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.