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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91000

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
October 24, 2022
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Tollos

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

Infection Control (IC) Lifting Strap used with the following Cirrus and Pinnacle Ceiling Lifts: Cirrus 450, Cirrus 600, Cirrus 700, Cirrus 750, and Pinnacle 1000

Z-0245-2023
Recall number
Z-0245-2023
Initiated
October 24, 2022
Classification
Class II
Status
Ongoing
Recalling firm
Tollos
Quantity
1273 US; 70 OUS

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Two customers reported four incidents in which the lifting strap broke while lifting a patient. If the IC strap fails during use, the patient may fall causing injury to them or the caregiver(s).

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Two customers reported four incidents in which the lifting strap broke while lifting a patient. If the IC strap fails during use, the patient may fall causing injury to them or the caregiver(s).

Code information

UDI-DI 00817956021 (not yet uploaded to GUDID)

Distribution pattern

Worldwide - US Nationwide distribution and the countries of Canada and United Arab Emirates.

Field note

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