Class ITerminatedVoluntary: Firm initiated

JFE FRANCHISING INC: food recall H-0200-2026

JFE FRANCHISING INC of Houston, TX recalled Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025. Reason: Peaches provided by Moonlight Peaches potentially contaminated with Listeria. The FDA listed it as Class I in its Enforcement Report dated Nov 19, 2025; distribution: Alabama, Arizona, Colorado, Idaho, Illinois, Indiana, Kansas, Kentucky, Michigan, Nebraska, Ohio, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wyoming.

Record status as published: Terminated (terminated Feb 6, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025
Product quantity
177 units/ 154.88lbs
Reason for recall
Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Codes, lots and dates on the package
Lots: CBMA341 DAL065 KH366 LV376 CBMA388 DAL088 KH367 LV394 CBMA506 DAL091 KH371 LV396 CBMA512 DAL096 KH389 LV397 CBMA593 DAL302 KH733 LV402 CBMA617 DAL318 KH738 LV713 CBMA819 DAL319 KH739 LV714 CBMA847 FM156 KH748 LV717 CBMA851 FM286 KMA209 LV718 CBMA881 FRYS615 KMA316 LV729 CBMA920 FRYS667 KMA334 LV734 CDMA411 FRYS698 KMA359 LV739 CDMA426 KD213 KMA401 LV744 CDMA435 KD546 KMA402 LV764 CDMA439 KD576 KMA504 LV776 CDMA468 KD584 KMA525 LV779 CDMA475 KD585 KMA554 LV785 CDMA482 KD594 KMA772 MI419 CDMA492 KD596 KS011 MI441 CDMA741 KD689 KS033 MI487 CDMA754 KH115 KS079 MI670 CDMA765 KH128 KS085 MI685 CDMA808 KH136 KS104 MI704 CDMA811 KH138 KS105 MI706 CDMA817 KH144 KS117 NAS526 CDMA836 KH146 KS118 NAS529 CDMA902 KH161 LV008 NAS570 CDMA923 KH179 LV014 NAS582 CDMA945 KH190 LV087 NAS628 CDMA951 KH307 LV224 NAS851 DAL015 KH308 LV292 NAS894 DAL034 KH310 LV339 SM030 DAL049 KH318 LV347 SM131 DAL054 KH346 LV352 SM136 DAL056 KH362 LV356 SM147 DAL061 KH363 LV371 SM475
Distribution pattern
AL, AZ, CO, ID, IL, IN, KS, KY, MI, NE, OH, TN, TX, UT, VA, WA, WV, WY
Recalling firm
JFE FRANCHISING INC, Houston, TX
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
E-Mail

Dates

EventDate
Recall initiated by the firmOct 29, 2025
Classified by the FDANov 19, 2025
Published in the Enforcement ReportNov 19, 2025
TerminatedFeb 6, 2026

Other recalls by JFE FRANCHISING INC

  • H-0639-2026 · Apr 8, 2026 · Class II — Foreign Object (Glass)
  • H-0638-2026 · Apr 8, 2026 · Class II — Foreign Object (Glass)
  • H-0209-2025 · Jul 9, 2025 · Class I — Cucumbers have the potential to be contaminated with Salmonella.
  • H-0208-2025 · Jul 9, 2025 · Class I — Cucumbers have the potential to be contaminated with Salmonella.
  • H-0207-2025 · Jul 9, 2025 · Class I — Cucumbers have the potential to be contaminated with Salmonella.
  • H-0206-2025 · Jul 9, 2025 · Class I — Cucumbers have the potential to be contaminated with Salmonella.
  • H-0205-2025 · Jul 9, 2025 · Class I — Cucumbers have the potential to be contaminated with Salmonella.
  • F-0590-2025 · Mar 12, 2025 · Class I — Potential to be contaminated with Salmonella
  • F-0589-2025 · Mar 12, 2025 · Class I — Potential to be contaminated with Salmonella
  • F-0588-2025 · Mar 12, 2025 · Class I — Potential to be contaminated with Salmonella

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0200-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.