Synergetics Recalls
37 recalls on record · October 30, 2013 to July 17, 2024 · Medical Devices
Recalls by year
13
14
16
24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 17, 2024Medical DevicesFDA
Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye
Hazard: Sterilization certificates could not be validated by the supplier
July 17, 2024Medical DevicesFDA
Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
Hazard: Sterilization certificates could not be validated by the supplier
July 17, 2024Medical DevicesFDA
Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)
Hazard: Sterilization certificates could not be validated by the supplier
July 17, 2024Medical DevicesFDA
Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Hazard: Sterilization certificates could not be validated by the supplier
October 26, 2016Medical DevicesFDA
Synergetics Inc recalls 25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in a Tyvek/Mylar double pouch configuration
Hazard: Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
October 26, 2016Medical DevicesFDA
Synergetics Inc recalls 25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator, Product/Part Number 70025SP, packaged in HIPS r
Hazard: Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
October 26, 2016Medical DevicesFDA
Synergetics Inc recalls 25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator, Product/Part Number 70025S, packaged in HIPS rigid tray
Hazard: Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
October 26, 2016Medical DevicesFDA
Synergetics Inc recalls 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS rigid tray with a Tyv
Hazard: Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 25ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.24.25P. Packed 12 units per box. Manufact
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 23ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.24.23P. Packed 12 units per box. Manufact
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 25ga Mid-Field Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.22.25P. Packed 12 units per box. Manufactu
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 23ga Mid-Field Endo Illuminator, Synergetics length 7.5 ft, sterile / EO, 56.22.23P. Packed 12 units per box. Manufactur
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls Stiff 25ga Wide Field Endo Illuminator, Synergetics, inc. length 7.5 ft, sterile / EO, 56.21.25PS. Packed 12 units per b
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 23ga Wide Field Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.21.23P. Packed 12 units per box. Ma
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls Wide Field Endo Illuminator, Vivid (tm) Endo Illuminator, 20ga, Synergetics, inc., 20ga, length 7.5 ft, sterile / EO, 56
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls Vivid (tm) Endo Illuminator, 20ga, Synergetics, inc., length 7.5 ft, sterile / EO, 56.20P. Packed 12 units per box. Manu
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls Two-Port Vitrectomy (TPV (tm)) Wide Field High Flow End Irrigator, Synergetics, inc., 19ga, length 7.0 ft, sterile / EO,
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 25ga Wide Field Corona Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.12.23P. Packed 12 units per
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 23ga Wide Field Corona Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.12.23P. Packed 12 units per
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls "The Corona" Shielded Wide Field Endo Illuminator, Synergetics, inc. 20ga, length 7.0 ft, sterile / EO, 56.12. Packed 12
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 27ga ONE-STEP (tm) Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.02.27P. Packed 12 units per box
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls Stiff 25ga Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.02.25PS. Packed 12 units per box. Manufa
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 25ga Endo Illuminator, Synergetics, inc., length 7.0 ft, sterile / EO, 56.02.25 Packed 12 units per box. Manufactured fo
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 23ga Endo Illuminator (Eckardt Trocar Compatible), Synergetics, inc., length 8.0 ft, sterile / EO, 56.02.23P Packed 12 u
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls Endo Illuminator, Synergetics, inc., 20ga, length 7.0 ft, sterile / EO, 56.02. Packed 12 units per box. Manufactured for
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 23ga Straight Fixed Extended Illuminated Laser Probe, Synergetics, length 7.5 ft, sterile / EO, 55.62.23P. Packed 12 uni
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 27ga ONE-STEP (tm) Awh/Tano Vivid Chandelier, Synergetics, length 8.0 ft, sterile / EO, 56.55.27P. Packed 12 units per b
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 25ga Awh Vivid Chandelier, Synergetics, length 7.5 ft, sterile / EO, 56.54.25P. Packed 12 units per box. Manufactured fo
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 25ga Awh Chandelier, Synergetics, inc., B&L Cannula Compatible, length 8.0 ft, sterile / EO, 56.52.25P. Packed 12 units
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
February 5, 2014Medical DevicesFDA
Synergetics Inc recalls 29ga Oshima Dual Chandelier, Synergetics, inc., length 7.5 ft, sterile / EO, 56.50.29P. Packed 12 units per box. Manufac
Hazard: Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.