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Family Health Products Inc., Omaha, Nebraska

Family Health Products Inc., Omaha, Nebraska Recalls

All product recalls associated with Family Health Products Inc., Omaha, Nebraska.

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Recall Summary

Total Recalls

1000

Past Year

897

Class I (Serious)

124

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 2101–2120 of 17593 recalls

Crystal Clear Sodium Hydroxide (Family Health) – Child Safety Issue (2023)

Fire/Burn Risk

This recall involves Family Health Products Crystal Clear Sodium Hydroxide products. Sodium hydroxide is commonly used for soapmaking and cleaning. The sodium hydroxide, also called lye or caustic soda, was sold in a resealable two-pound bag with "CRYSTAL CLEAR", "SODIUM HYDROXIDE", "Protect, Deliver, Clean", and "NaOH" printed in large type.

Moderate

CPSCOct 12, 2023Nationwide• Family Health Products Inc., Omaha, Nebraska

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)

1...104 105106107 108...880

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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

Radiology Solutions (Change Healthcare) – record update issue (2023)

Change Healthcare has identified a software issue where Change Healthcare Radiology Solutions 14.0, 14.1, and 14.2 may not update records in external applications.

Low

FDAOct 12, 2023Nationwide• CHANGE HEALTHCARE CANADA COMPANY

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

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.

Moderate

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

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

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

D-Clip Applier (Peter Lazic) – Surgery Failure Risk (2023)

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

Moderate

FDAOct 6, 2023Nationwide• Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany

ORION System (LEONI) – Unintended Movement Risk (2023)

Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.

High

FDAOct 6, 2023Nationwide• LEONI CIA CABLE SYSTEMS 5 avenue Victor Hugo Chartres France

D-Clip Applier (Peter Lazic) – Surgery Failure Risk (2023)

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

Moderate

FDAOct 6, 2023Nationwide• Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany

Favorite Day Demi French Bread (Rise Baking) – Foreign material (2023)

Foreign Material (plastic).

Class IIModerate

FDAOct 5, 2023CA, IA• Rise Baking Company, LLC dba The New French Bakery Inc.

BD Insyte IV Catheter (Becton Dickinson) – Needle Retraction Issue (2023)

Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and repeat catheter insertion attempts, due to catheter being inadvertently removed from the insertion site.

High

FDAOct 4, 2023Nationwide• Becton Dickinson Infusion Therapy Systems Inc.

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.

High

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.

Moderate

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