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La Michoacana 100% Natural Inc

La Michoacana 100% Natural Inc Recalls

All product recalls associated with La Michoacana 100% Natural Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 3241–3260 of 21320 recalls

Ice Cream Bar Michoacana (La Michoacana) – Undeclared Dyes (2023)

Undeclared Allergen

Undeclared Yellow #5, Yellow #6, and Red #40

Class IIModerate

FDAOct 16, 2023FL• La Michoacana 100% Natural Inc

MPV Circuit Kit (Breas Medical) – ventilation risk (2023)

Produced with unintended open slits on the side of the mouthpiece body, may result in insufficient ventilation in spontaneous breathing patients using MPV-VCV and MPV-PCV modes of ventilation

High

FDAOct 13, 2023Nationwide• Breas Medical, Inc.

BALLARD Closed Suction System (Avanos) – DEHP labeling error (2023)

Certain lots of BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI were labeled as not being made with Di(2-ethylhexyl) phthalate (DEHP); however, Avanos has determined that the tubing components of the product did contain DEHP.

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Moderate

FDAOct 13, 2023Nationwide• Avanos Medical, Inc.

Cardiohelp-i System (Maquet) – weld defect (2023)

It was found that the fixation (weld) employed by the supplier of the nut bolt to the slide rail plate was insufficient. The deficient weld allows the nut bolt to break off from the slide rail plate with slight manual force.

High

FDAOct 12, 2023Nationwide• Maquet Medical Systems USA

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.

High

FDAOct 12, 2023Nationwide• Olympus Corporation of the Americas

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

High

FDAOct 12, 2023Nationwide• Olympus Corporation of the Americas

Mo.Ma Ultra Device (Medtronic) – labeling issue (2023)

The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and superior sticker, one on each side of the manifold. These stickers label the common carotid artery (CCA) proximal balloon and external carotid artery (ECA) distal balloon inflation and deflation ports. Both sides of the complaint units manifold were labelled with the superior label leading to an incorrect identification of the proximal and distal inflation /deflation ports when viewing the devices from the inferior side.

High

FDAOct 12, 2023Nationwide• Medtronic Inc

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

High

FDAOct 12, 2023Nationwide• Olympus Corporation of the Americas

Bronchovideoscope (Olympus) – combustion risk (2023)

High

FDAOct 12, 2023Nationwide• Olympus Corporation of the Americas

VariSoft Infusion Set (Unomedical A/S) – Connector Damage (2023)

The Varisoft infusion set is used in conjunction with tandem insulin pumps. The defect reported was damage to the connector piece during manufacturing. This damage results in the connector becoming detached more easily from the insulin set than expected, requiring less force to disconnect than intended. Disconnection, when not detected, for example during sleep, leads to missed basal dosing. which in turn can result in elevated blood glucose and ketone level (nocturnal hyperglycemia). Diabetic ketoacidosis.

High

FDAOct 11, 2023Nationwide• Unomedical A/S Aaholmvej

BD Alaris Pump Infusion Sets (Becton Dickinson) – DEHP Mislabeling (2023)

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

Moderate

FDAOct 11, 2023Nationwide• Becton Dickinson & Company

BD Extension Sets (Becton Dickinson) – DEHP Mislabeling (2023)

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

Moderate

FDAOct 11, 2023Nationwide• Becton Dickinson & Company

BD Gravity Sets (Becton Dickinson) – DEHP Mislabeling (2023)

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

Moderate

FDAOct 11, 2023Nationwide• Becton Dickinson & Company

VITROS 5600 System (Ortho-Clinical) – Software Issues (2023)

During planned monitoring of data post-release of Software Version 3.8.0 an increased occurrence of software issues relating to unresponsive subsystems, unresponsive user interface (sometimes referred to as a screen freeze), and/or printer disconnections was identified. The consequence of these issues would be a delay in reporting results due to the required system shutdowns to recover the system. This delay in reporting results could occur during any assay, including which the speed of the result is deemed critical or STAT and could result in a delay of treatment in a patient. Due to the release strategy of this software version, the user could not update the system but a field engineer had to manually install each affected system.

Moderate

FDAOct 10, 2023Nationwide• Ortho-Clinical Diagnostics, Inc.

Stay Safe Cap (Fresenius Medical) – Additional Warnings (2023)

Updating the labeling to include additional warnings and contraindications for potential side effects.

Moderate

FDAOct 10, 2023Nationwide• Fresenius Medical Care Holdings, Inc.

CARDIOHELP Emergency Drive (Maquet) – Patient Exposure Risk (2023)

Product removal due to possible blocking or impairment of the CARDIOHELP Emergency Drive. This issue can lead to the patient being exposed to inappropriate low blood flow. Potential associated harms are ischemia and hypoxia.

High

FDAOct 10, 2023Nationwide• Maquet Medical Systems USA

Stay Informed

La Michoacana 100% Natural Inc Recalls

Recall Summary

Ice Cream Bar Michoacana (La Michoacana) – Undeclared Dyes (2023)

MPV Circuit Kit (Breas Medical) – ventilation risk (2023)

BALLARD Closed Suction System (Avanos) – DEHP labeling error (2023)

Cardiohelp-i System (Maquet) – weld defect (2023)

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

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

Mo.Ma Ultra Device (Medtronic) – labeling issue (2023)

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

Bronchovideoscope (Olympus) – combustion risk (2023)

VariSoft Infusion Set (Unomedical A/S) – Connector Damage (2023)

BD Alaris Pump Infusion Sets (Becton Dickinson) – DEHP Mislabeling (2023)

BD Extension Sets (Becton Dickinson) – DEHP Mislabeling (2023)

BD Gravity Sets (Becton Dickinson) – DEHP Mislabeling (2023)

VITROS 5600 System (Ortho-Clinical) – Software Issues (2023)

Stay Safe Cap (Fresenius Medical) – Additional Warnings (2023)

CARDIOHELP Emergency Drive (Maquet) – Patient Exposure Risk (2023)

VITROS XT 7600 System (Ortho-Clinical) – Software Issues (2023)

VITROS 4600 System (Ortho-Clinical) – Software Issues (2023)

VITROS 3600 System (Ortho-Clinical) – Software Issues (2023)

VITROS XT 3400 System (Ortho-Clinical) – Software Issues (2023)