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Pacific International Marketing

Pacific International Marketing Recalls

All product recalls associated with Pacific International Marketing.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 101–120 of 4099 recalls

Fresh Herbs (Pacific International) – Salmonella Risk (2025)

Salmonella

Potential contamination with Salmonella.

Class IHigh

FDAOct 27, 2025AZ, CA, FL +5 more• Pacific International Marketing

Vegetable Carton Label (Pacific International) – Salmonella Risk (2025)

Salmonella

Potential contamination with Salmonella.

Class IHigh

FDAOct 27, 2025AZ, CA, FL +5 more• Pacific International Marketing

IntelePACS (Intelerad) – Software Communication Bug (2025)

Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss in Relevant Clinical Info field when modifying studies through Case Editor in either Technologist Portal or Referring Physician Portal, which could result in loss of clinical information, which could impact clinical decision-making.

1...4 567 8...205

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Moderate

FDAOct 17, 2025Nationwide• INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

Multichem ID-B (Techno-Path) – HBsAg Recovery Issue (2025)

Potential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform.

Moderate

FDAOct 17, 2025CA, CO, CT +14 more• TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

EZDilate Nephrostomy Catheter (Olympus) – Incorrect Balloon Size (2025)

Device kits contained an incorrectly sized 4mm x 4cm urinary tract balloon catheter (BURS0404) instead of the correct 8mm x 15cm nephrostomy tract balloon catheter (BPCN0815). All other components in the kits were correctly included and packaged in the kit.

Moderate

FDAOct 17, 2025AK, CA, IA +3 more• Olympus Corporation of the Americas

Cinnamon Whiskey Pecans (Nats Nuts) - Undeclared Cashews (2025)

Undeclared Allergen

Contains undeclared cashews

Class IIModerate

FDAOct 16, 2025CT, FL, NV +6 more• Nats Nuts LLC

Ceiling Type X-Ray Tube Support (Shimadzu) – Mounting Shaft Risk (2025)

Due to an issue (potential breakage) with the shaft for the mounting of the X-ray tube assembly that could potentially result assembly coming off the rotating shaft.

High

FDAOct 16, 2025Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

EVIS EXERA III Duodenovideoscope (Olympus) – Reprocessing Update (2025)

Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes, reminding users to closely follow the operation and reprocessing instructions, and providing updated materials to users.

Moderate

FDAOct 14, 2025Nationwide• Olympus Corporation of the Americas

Olopatadine Ophthalmic Solution (USV) – Impurity Concern (2025)

Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.

Class IIModerate

FDAOct 9, 2025Nationwide• USV Private Limited

ShockPulse Lithotripsy Transducer (Olympus) – startup failure (2025)

The device may either fail to start up, or the transducer may start briefly and then stop, accompanied by an error light on the generator. In addition, the body of the transducer handpiece may gradually increase in temperature during clinical use.

Moderate

FDAOct 8, 2025Nationwide• Olympus Corporation of the Americas

Single Use Electrosurgical Snare (Olympus) – sterility compromise (2025)

Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.

Moderate

FDAOct 6, 2025Nationwide• Olympus Corporation of the Americas