PlainRecalls

SEDECAL SA

32 recalls on record · Latest: Oct 29, 2025

SEDECAL SA Recall Insight

SEDECAL SA appears on 32 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.038% 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 Oct 29, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 32 entries, severity tagging shows 0 critical, 32 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 31 of 32 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 (32). The date window on this page runs from Mar 8, 2023 to Oct 29, 2025.

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 Oct 29, 2025

MobileDiagnost wDR 2.2; Model Number REF 9890-010-89522, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-32HF-B-D-C; 32KW 50G, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number 40KWFXPLUS.004, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW 70C, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

SM_40HF_B_D_VIR3, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

SM_40HF_BDC3, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-20HF-Batt; 20KW ANALOG, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

SHIMADZU RF.004, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW.002, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number 40KW-FX.899, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number 40KWFXPLUS-710CW.007, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model SM-40HF-B-D-C; 40KW - CANON READY, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW.005, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

SM_40HF_B_D_VIR3.004, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number 40KWFXPLUS.889, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW 55C, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW 55G/60G, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

SM_40HF_BDC, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

RADPRO MOBILE, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Sedecal Mobile Digital Diagnostic X-Ray Systems; SM-40HF-B-D-KM (AeroDR X30)

FDA Devices Moderate Oct 29, 2025

Model Number 40KWMOBILE3.899, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number 40KWFXPLUS.005, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW 80C, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number 40KWFXPLUS.002, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Model Number SM-40HF-B-D-C; 40KW 55G, Mobile X-ray system

FDA Devices Moderate Oct 29, 2025

Sedecal Easy Moving Plus Model Number SM-50HF-B-D-C; 50KW 50G, Mobile X-ray system

FDA Devices Moderate May 8, 2024

Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1, model numbers: a. SM-20HF-Batt; b. SM-32HF-Batt; c. SM-40HF-Batt; d.…

FDA Devices Moderate Feb 21, 2024

MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007

FDA Devices Moderate Jan 31, 2024

Sedecal X Optima URS digital mobile diagnostic x-ray system. A a stationary x-ray unit with a universal swivel arm. It allows one to take expos…

FDA Devices Moderate Mar 8, 2023

Phoenix mKDR Xpress, digital mobile diagnostic x-ray system

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

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