Paragon 28, Inc. recalls
4 recalls filed under Paragon 28, Inc.. The most recent was published August 26, 2026.
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Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
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Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Small Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
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Class II · 3 months ago
Paragon 28, Inc. P28 Phanton Intramedullary Nail System, Phantom Hindfoot TTC/TC Ball recall: Paragon 28 received two (2) complaints were received involving breaches
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
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Class II · 11 months ago
Paragon 28, Inc. Phantom recall: Fibula nail system intended for use in fixation of fibular fractures
Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so…
About this page
Paragon 28, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.