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Nature'S Path Foods Inc

Nature'S Path Foods Inc Recalls

All product recalls associated with Nature'S Path Foods Inc.

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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 561–580 of 4099 recalls

Dark Chocolate Chip Waffles (Nature's Path) – Undeclared Peanut (2023)

Undeclared Nuts

undeclared peanut

Class IIModerate

FDAOct 19, 2023CA, CO, CT +14 more• Nature'S Path Foods Inc

Pumpkin Spice Waffles (Nature's Path) – Undeclared Peanut (2023)

Undeclared Nuts

undeclared peanut

Class IIModerate

FDAOct 19, 2023CA, CO, CT +14 more• Nature'S Path Foods Inc

EVIS EXERA II Bronchovideoscope (Olympus) – combustion risk (2023)

There is a risk of endobronchial combustion if high-frequency cauterization is performed while supplying oxygen [and/or] the electrode section of the electrosurgical accessory is too close to the distal end of the endoscope.

1...27 282930 31...205

Page 29 of 205Next

FDAOct 12, 2023Nationwide• Olympus Corporation of the Americas

RANDOX Total Bilirubin (Randox Laboratories) – Elevated Patient Results (2023)

Randox has had reports of elevated patient results using Plasma (lithium heparin) samples with Total Bilirubin reagent (TBil) Vanadate Oxidation Method.

FDAOct 11, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

EVIS EXERA III Videoscope (Olympus) – Sterilization Failure (2023)

Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel.

FDAOct 2, 2023Nationwide• Olympus Corporation of the Americas

ACMI Roller Bar Electrodes (Olympus) – Incorrect Pouch Labeling (2023)

Incorrect pouch labels, the contents within the mislabeled pouch were Roller Bar electrodes.

FDAOct 2, 2023AL, FL, GA +10 more• Olympus Corporation of the Americas

GEM Premier 3000 PAK (Instrumentation) – pO2 Over-Recovery (2023)

Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications for pO2. The positive bias may lead to false positive for medical decision levels at pO2 < 60 mmHg, which may result in failure to detect and/or adequately treat hypoxemia and lead to a delay in treatment. The quality control procedures for the Non-iQM GEM Premier 3000 may not detect the non-conformance.

FDASep 29, 2023MA, MN, NY• Instrumentation Laboratory

Atrium Thoracic Catheter (Atrium) – Expiration Date Error (2023)

A sterilization nonconformance prematurely aged the product, resulting in an inaccurate labeled expiration date.

FDASep 29, 2023AL, AZ, CA +11 more• Atrium Medical Corporation

Liposomal Multivitamins (Solaray) – Packaging concern (2023)

This recall involves Solaray Liposomal Women's in 60 and 120 count, Solaray Universal Multivitamin in 60 and 120 count, and Solaray Liposomal Women's 50+ Multivitamin in 120 count. The bottles are a clear silver color with white pop top lids. The white label on the front of the bottles displays the Solaray logo, product name, product type and size count. The 60 count bottles are contained in cartons, which are substantially similar in appearance to the bottles inside. All lots are included in the recall. Name Count SKU Solaray Liposomal Women's 60 076280193251 Solaray Liposomal Women's 120 076280339536 Solaray Universal Multivitamin 60 076280640168 Solaray Universal Multivitamin 120 076280830385 Solaray Liposomal Women's 50+ Multivitamin 120 076280154832

CPSCSep 28, 2023Nationwide• Nutraceutical Corporation, of Salt Lake City, Utah

Tracheal Intubation Fiberscope (Olympus) – Flow Rate Issue (2023)

Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.

FDASep 28, 2023Nationwide• Olympus Corporation of the Americas

SENTIERO Medical Device (PATH) – Technical Distortion (2023)

Affected lots of product may experience technical distortions to a greater extent than expected.

FDASep 26, 2023FL, MO, OH +1 more• PATH Landsberger Str. 65 Germering Germany

SENTIERO Screening2 (PATH) – Technical Distortion (2023)

Affected lots of product may experience technical distortions to a greater extent than expected.

FDASep 26, 2023FL, MO, OH +1 more• PATH Landsberger Str. 65 Germering Germany

AuDX PRO Medical Device (PATH) – Technical Distortion (2023)

Affected lots of product may experience technical distortions to a greater extent than expected.

FDASep 26, 2023FL, MO, OH +1 more• PATH Landsberger Str. 65 Germering Germany

SENTIERO Screening (PATH) – Technical Distortion (2023)

Affected lots of product may experience technical distortions to a greater extent than expected.

FDASep 26, 2023FL, MO, OH +1 more• PATH Landsberger Str. 65 Germering Germany

Insufflation Unit (Olympus) – Air Supply Stoppage (2023)

Olympus has become aware of an increased trend of both repairs and customer complaints reporting "UHI-4 stopping air supply due to the front panel LED turning off".

FDASep 25, 2023Nationwide• Olympus Corporation of the Americas

High-Flow Insufflation Unit (Olympus) – Cardiac Arrest Risk (2023)

There have been reports of patients suffering arrhythmias, reported as short cardiac arrests, during surgical procedures where UHI-4s were used. These events may have been due to an over insufflation of the abdominal cavity resulting from use of the UHI-4 during the procedures.

FDASep 22, 2023Nationwide• Olympus Corporation of the Americas

Advanta V12 Stent (Atrium) – Balloon Weld Failure (2023)

Balloon-to-catheter weld failure that may cause loss of balloon pressure during stent deployment.

FDASep 21, 2023Nationwide• Atrium Medical Corporation

Stay Informed

Nature'S Path Foods Inc Recalls

Recall Summary

Dark Chocolate Chip Waffles (Nature's Path) – Undeclared Peanut (2023)

Pumpkin Spice Waffles (Nature's Path) – Undeclared Peanut (2023)

EVIS EXERA II Bronchovideoscope (Olympus) – combustion risk (2023)

EVIS EXERA b Bronchovideoscope (Olympus) – combustion risk (2023)

EVIS EXERA III Bronchovideoscope (Olympus) – combustion risk (2023)

Bronchovideoscope (Olympus) – combustion risk (2023)

RANDOX Total Bilirubin (Randox Laboratories) – Elevated Patient Results (2023)

EVIS EXERA III Videoscope (Olympus) – Sterilization Failure (2023)

ACMI Roller Bar Electrodes (Olympus) – Incorrect Pouch Labeling (2023)

GEM Premier 3000 PAK (Instrumentation) – pO2 Over-Recovery (2023)

Atrium Thoracic Catheter (Atrium) – Expiration Date Error (2023)

Liposomal Multivitamins (Solaray) – Packaging concern (2023)

Tracheal Intubation Fiberscope (Olympus) – Flow Rate Issue (2023)

SENTIERO Medical Device (PATH) – Technical Distortion (2023)

SENTIERO Screening2 (PATH) – Technical Distortion (2023)

AuDX PRO Medical Device (PATH) – Technical Distortion (2023)

SENTIERO Screening (PATH) – Technical Distortion (2023)

Insufflation Unit (Olympus) – Air Supply Stoppage (2023)

High-Flow Insufflation Unit (Olympus) – Cardiac Arrest Risk (2023)

Advanta V12 Stent (Atrium) – Balloon Weld Failure (2023)