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Given Imaging Ltd. New Industrial Park

Given Imaging Ltd. New Industrial Park Recalls

All product recalls associated with Given Imaging Ltd. New Industrial Park.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 1221–1240 of 37661 recalls

Bravo CF Capsule Device (Given Imaging) – Adhesive Malfunction (2025)

It has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule from attaching to the patient's esophagus or detaching from the delivery device.

FDAJun 3, 2025Nationwide• Given Imaging Ltd. New Industrial Park

BD FACS Setup Beads (Becton Dickinson) – Spectral Overlap Error (2025)

Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.

FDAJun 3, 2025AZ, AR, CA +34 more• Becton, Dickinson and Company, BD Bio Sciences

Battle Motors LET2 (Battle Motors) – Steering Nut Problem (2025)

Battle Motors, Inc. (Battle Motors) is recalling certain 2024-2025 Let2 trucks. The steering wheel retaining nut may have been improperly tightened, allowing the steering wheel to loosen and detach from the steering shaft.

1...60 616263 64...1884

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Very High

NHTSAJun 2, 2025Nationwide• BATTLE MOTORS

Pizza Shoppe Pink Stuff Garlic Dressing (La Fontanella) – Potential Spoilage (2025)

Potential for product spoilage (increased level of lactic acid detected in retain samples).

Class IIModerate

FDAJun 2, 2025IN, IA, KS +1 more• La Fontanella Food Products LLC

Lidocaine HCL Sterile Injection (Tailstorm Health) – Sterility Concerns (2025)

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Class IIModerate

FDAJun 2, 2025Nationwide• Tailstorm Health INC

Ketamine Hydrochloride 50mg Injection (Tailstorm Health) – Sterility Concerns (2025)

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Class IIModerate

FDAJun 2, 2025Nationwide• Tailstorm Health INC

Lidocaine HCL with Epinephrine Injection (Tailstorm Health) – Sterility Concerns (2025)

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Class IIModerate

FDAJun 2, 2025Nationwide• Tailstorm Health INC

Ketamine Hydrochloride Injection (Tailstorm Health) – Sterility Concerns (2025)

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Class IIModerate

FDAJun 2, 2025Nationwide• Tailstorm Health INC

Bupivacaine HCL Sterile Injection (Tailstorm Health) – Sterility Concerns (2025)

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Class IIModerate

FDAJun 2, 2025Nationwide• Tailstorm Health INC

Lidocaine HCl Injection (Tailstorm Health) – Sterility Concerns (2025)

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Class IIModerate

FDAJun 2, 2025Nationwide• Tailstorm Health INC

Eudos Bronquilan (Nature's Eudos) – Undeclared Colors (2025)

Undeclared Allergen

Undeclared colors (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40)

Class IIModerate

FDAJun 1, 2025NJ, NY• Nature's Eudos Distributors LLC

Platelia Toxo IgM (Bio-Rad) – False Positive Results (2025)

Due to a risk of false positive results that could lead to unnecessary medical treatment.

FDAMay 30, 2025Nationwide• Bio-Rad Laboratories, Inc.

Servo-u MR Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen

Hillrom Q-Link 13 Component (Baxter Healthcare) – False Attachment Risk (2025)

The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.

FDAMay 30, 2025Nationwide• Baxter Healthcare Corporation

Servo-u Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen

Hillrom LikoScale (Baxter) – Attachment Hook Risk (2025)

The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.

FDAMay 30, 2025Nationwide• Baxter Healthcare Corporation

Inseego USB8 4G Dongle Kit (Remote Diagnostic) – Outdated Software (2025)

Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead to delay in diagnosis, delayed treatment, hypoxia due to unexpected loss of video laryngoscopy and all other monitor measurements during system restart.

FDAMay 30, 2025Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

Testo-200 Testosterone Injection (Advanced Pharma) – Unapproved Product (2025)

Marketed Without an Approved NDA/ANDA

Class IIModerate

FDAMay 30, 2025NJ, NY• Advanced Pharmaceutical Technology, Inc.

Collins Bus (Forest River) – Emergency Exit Failure (2025)

Forest River Bus, LLC (Forest River Bus) is recalling certain 2025 Collins Bus transit buses. The lock on the emergency exit door may fail to unlock. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 217, "Bus Emergency Exits and Window Retention and Release."

NHTSAMay 30, 2025Nationwide• FOREST RIVER BUS

Servo-n Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen