Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Device

BIOPSYBELL S.R.L.: Products labeled as sterile were distributed, but may not have been sterilized.

Agency Publication Date: May 19, 2021
Share:
Sign in to monitor this recall

Affected Products

Product: BPB medica CEMIX, PRODUCT NUMBER KVTMIXN, Vertebroplasty-Kyphoplasty cement mixing system

BATCH: 19123253

Lot Numbers:
19123253
Product: RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE, RESFIL1112C1-US

BATCH: 20061305

Lot Numbers:
20061305
Product: BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP, 187 mm, 10G, RES RESWTR1112C-US

BATCH: 20061307

Lot Numbers:
20061307
Product: BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT, 110 mm, 11 G, REF OBE1111

BATCH Numbers: 20061439

Lot Numbers:
Numbers
Product: CEMENT MIXING SYSTEM, VERTEBROPLASTY-KYPHOPLASTY, REF VCF-1051

BATCH:2003721

Lot Numbers:
2003721
Product: EASYNJECT, Device for cement infusion in the vertebroplasty procedure, REF KVTGUN-DS

BATCH:2003721

Lot Numbers:
2003721
Product: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKBD

LOT: 19102741, 200127, 2001246, 2101242

Lot Numbers:
19102741
Product: 10 GAUGE CEMENT DELIVERY CANNULA, CODE INTVM-CDC

LOT: 19112827, 2002440

Lot Numbers:
19112827
Product: 10G DIRECT SINGLE - ACCESS, CODE INTVM-DSBAK

LOT: 2001201, 2003859, 20051288, 20061419

Lot Numbers:
2001201
Product: 8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTVM-DWCB

LOT: 20061432

Lot Numbers:
20061432
Product: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES), CODE INTVMN-SCDK

LOT: 2001185, 2001243, 20051163

Lot Numbers:
2001185
Product: CEMIX - CEMENT MIXING SYSTEM, CODE INTV-MMS

LOT: 2001185, 2001243, 20051163

Lot Numbers:
2001185
Product: 11G DIRECT WORKING CANNULA DIAMOND TIP MINI, CODE INTVMN-DWCD

LOT: 2002437

Lot Numbers:
2002437
Product: 11G DIRECT SINGLE - ACCESS, CODE INTVMN-DSBAK

LOT: 20051162

Lot Numbers:
20051162
Product: 8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTV-DWCB

LOT: 30061432

Lot Numbers:
30061432
Product: 10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES, CODE INTVM-SCDK

LOT: 2002439, 20051290, 20061420, 20081943

Lot Numbers:
2002439
Product: 10G DIRECT WORKING CANNULA BEVEL TIP 15CM, CODE INTVM-DWCB/15

LOT: 20071561

Lot Numbers:
20071561
Product: 10G COAXIAL CANNULA WITH TUOHY CONNECTION, CODE INTVM-CC

LOT: 20102495

Lot Numbers:
20102495
Product: 10 GAUGE DRILL, CODE INTVM-DRL

LOT: 20102486

Lot Numbers:
20102486

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87696
Status: Resolved
Manufacturer: BIOPSYBELL S.R.L.
Manufactured In: Italy
Units Affected: 19 products (5 units; 60 units; 10 units; 50 units; 500 units; 5 units; 625 units; 250 units; 330 units; 30 units; 160 units; 1000 units; 75 units; 50 units; 30 units; 305 units; 50 units; 40 units; 75 units)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.