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BIOPSYBELL S.R.L Recalls
19 recalls on record · May 26, 2021 to May 26, 2021 · Medical Devices
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10 GAUGE DRILL, CODE INTVM-DRL
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10G COAXIAL CANNULA WITH TUOHY CONNECTION, CODE INTVM-CC
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10G DIRECT WORKING CANNULA BEVEL TIP 15CM, CODE INTVM-DWCB/15
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES, CODE INTVM-SCDK
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTV-DWCB
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 11G DIRECT SINGLE - ACCESS, CODE INTVMN-DSBAK
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 11G DIRECT WORKING CANNULA DIAMOND TIP MINI, CODE INTVMN-DWCD
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls CEMIX - CEMENT MIXING SYSTEM, CODE INTV-MMS
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES), CODE INTVMN-SCDK
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTVM-DWCB
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10G DIRECT SINGLE - ACCESS, CODE INTVM-DSBAK
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10 GAUGE CEMENT DELIVERY CANNULA, CODE INTVM-CDC
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKBD
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls EASYNJECT, Device for cement infusion in the vertebroplasty procedure, REF KVTGUN-DS
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls CEMENT MIXING SYSTEM, VERTEBROPLASTY-KYPHOPLASTY, REF VCF-1051
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT, 110 mm, 11 G, REF OBE1111
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP, 187 mm, 10G, RES RESWTR1112C-US
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE, RESFIL1112C1-US
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.
May 26, 2021Medical DevicesFDA
BIOPSYBELL S.R.L. recalls BPB medica CEMIX, PRODUCT NUMBER KVTMIXN, Vertebroplasty-Kyphoplasty cement mixing system
Hazard: Products labeled as sterile were distributed, but may not have been sterilized.