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Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan

Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan Recalls

All product recalls associated with Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan.

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Recall Summary

Total Recalls

1000

Past Year

589

Class I (Serious)

65

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 3921–3940 of 10393 recalls

SnareMaster Plus (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

Cannula (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.

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Moderate

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

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

Extraction Balloon (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

Aspiration Needle (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

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

Injector ForceMax Lower 23G (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

Biliary Stent (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 6mm 25G 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

NeedleMaster 6mm 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

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

NeedleMaster 6mm 23G 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

Biliary Stent (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

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

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