PlainRecalls

Biopsybell S.r.l.

19 recalls on record · Latest: May 26, 2021

Biopsybell S.r.l. Recall Insight

Biopsybell S.r.l. appears on 19 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.019% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 26, 2021, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 19 entries, severity tagging shows 0 critical, 19 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 19 of 19 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (19). The date window on this page runs from May 26, 2021 to May 26, 2021.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate May 26, 2021

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

FDA Devices Moderate May 26, 2021

11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES), CODE INTVMN-SCDK

FDA Devices Moderate May 26, 2021

11G DIRECT SINGLE - ACCESS, CODE INTVMN-DSBAK

FDA Devices Moderate May 26, 2021

CEMENT MIXING SYSTEM, VERTEBROPLASTY-KYPHOPLASTY, REF VCF-1051

FDA Devices Moderate May 26, 2021

RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE, RESFIL1112C1-US

FDA Devices Moderate May 26, 2021

10G DIRECT SINGLE - ACCESS, CODE INTVM-DSBAK

FDA Devices Moderate May 26, 2021

BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT, 110 mm, 11 G, REF OBE1111

FDA Devices Moderate May 26, 2021

10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKBD

FDA Devices Moderate May 26, 2021

10G DIRECT WORKING CANNULA BEVEL TIP 15CM, CODE INTVM-DWCB/15

FDA Devices Moderate May 26, 2021

8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTVM-DWCB

FDA Devices Moderate May 26, 2021

10 GAUGE DRILL, CODE INTVM-DRL

FDA Devices Moderate May 26, 2021

BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP, 187 mm, 10G, RES RESWTR1112C-US

FDA Devices Moderate May 26, 2021

8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTV-DWCB

FDA Devices Moderate May 26, 2021

10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES, CODE INTVM-SCDK

FDA Devices Moderate May 26, 2021

EASYNJECT, Device for cement infusion in the vertebroplasty procedure, REF KVTGUN-DS

FDA Devices Moderate May 26, 2021

10G COAXIAL CANNULA WITH TUOHY CONNECTION, CODE INTVM-CC

FDA Devices Moderate May 26, 2021

10 GAUGE CEMENT DELIVERY CANNULA, CODE INTVM-CDC

FDA Devices Moderate May 26, 2021

CEMIX - CEMENT MIXING SYSTEM, CODE INTV-MMS

FDA Devices Moderate May 26, 2021

11G DIRECT WORKING CANNULA DIAMOND TIP MINI, CODE INTVMN-DWCD

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.