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Natus Manufacturing Limited Ida Business Park Glenbrack Road Galway Ireland

Natus Manufacturing Limited Ida Business Park Glenbrack Road Galway Ireland Recalls

All product recalls associated with Natus Manufacturing Limited Ida Business Park Glenbrack Road Galway Ireland.

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Recall Summary

Total Recalls

1000

Past Year

888

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 5441–5460 of 17593 recalls

Natus EDS CSF Drainage (Natus) - Pyrogen Test Failure (2021)

The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.

FDAJan 12, 2021Nationwide• Natus Manufacturing Limited Ida Business Park Glenbrack Road Galway Ireland

Phytonadione Tablets (Bausch) – Impurity Specification (2021)

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

FDAJan 7, 2021Nationwide• Bausch Health Companies, Inc.

Mephyton Tablets (Bausch) – Impurity Specification (2021)

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

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FDAJan 7, 2021Nationwide• Bausch Health Companies, Inc.

Klein's Cookies and Cream Bulk Ice Cream (Weis Markets) – Metal Contamination (2021)

Ice Cream product may contain metal (foreign objects).

Class IIModerate

FDAJan 5, 2021DE, IN, MD +5 more• Weis Markets, Inc., Ice Cream Division

Weis Quality Cookies and Cream Ice Cream – Metal Contamination (2021)

Ice Cream product may contain metal (foreign objects).

Class IIModerate

FDAJan 5, 2021DE, IN, MD +5 more• Weis Markets, Inc., Ice Cream Division

Klein's Vanilla Ice Cream (Weis Markets) – Metal Contamination (2021)

Ice Cream product may contain metal (foreign objects).

Class IIModerate

FDAJan 5, 2021DE, IN, MD +5 more• Weis Markets, Inc., Ice Cream Division

Nelsons Graham Slam Bulk Ice Cream (Weis Markets) – Metal Contamination (2021)

Ice Cream product may contain metal (foreign objects).

Class IIModerate

FDAJan 5, 2021DE, IN, MD +5 more• Weis Markets, Inc., Ice Cream Division

Balloon Catheter (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Electrosurgical Snare (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Guide Sheath Kit (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Replacement Basket (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

NeedleMaster 1.8mm 26G Lower (Aomori Olympus) – Sterile Seal Issue (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Injector ForceMax (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Injector ForceMax (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Electrosurgical Snare (Olympus) - Package Seal Defect (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

NeedleMaster 4mm 25G Upper (Aomori Olympus) – Sterile Seal Issue (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Aspiration Needle ViziShot (Aomori Olympus) – Sterile Seal Issue (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Aspiration Needle (Aomori Olympus) – Sterile Seal Issue (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

NeedleMaster 4mm 23G Upper (Aomori Olympus) – Sterile Seal Issue (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

NeedleMaster 5mm 21G Upper (Aomori Olympus) – Sterile Seal Issue (2021)

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

FDAJan 4, 2021Nationwide• Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan