Synergetics Inc recalls

8 recalls on record · latest: June 12, 2024

Official U.S. recall history for Synergetics Inc, compiled from official government records.

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Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)

June 12, 2024 · Medical device recalls High risk Sterilization certificates could not be validated by the supplier

Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)

June 12, 2024 · Medical device recalls High risk Sterilization certificates could not be validated by the supplier

Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)

June 12, 2024 · Medical device recalls High risk Sterilization certificates could not be validated by the supplier

Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)

June 12, 2024 · Medical device recalls High risk Sterilization certificates could not be validated by the supplier

Synergetics Inc recalls 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS rigid tray with a Ty…

August 11, 2016 · Medical device recalls Moderate risk Vitrectomy cutters have been found not to be operating within the correct press…

Synergetics Inc recalls 25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator, Product/Part Number 70025SP, packaged in HIPS…

August 11, 2016 · Medical device recalls Moderate risk Vitrectomy cutters have been found not to be operating within the correct press…

Synergetics Inc recalls 25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in a Tyvek/Mylar double pouch configuratio…

August 11, 2016 · Medical device recalls Moderate risk Vitrectomy cutters have been found not to be operating within the correct press…

Synergetics Inc recalls 25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator, Product/Part Number 70025S, packaged in HIPS rigid tra…

August 11, 2016 · Medical device recalls Moderate risk Vitrectomy cutters have been found not to be operating within the correct press…