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Terminated

Stryker brand Birthing Bed; Model 4701.

FDA Recall Z-0793-05 · Posted 2005-05-03

Recalling FirmStryker Medical
Recall StatusTerminated
Product CodeHDD
Date Initiated2005-03-31
Date Terminated2005-05-09
Product Quantity31

Reason for Recall

Trendelenburg and reverse trendelenburg features may not function.

Firm Action

Consignees were notified via letter dated 3/31/05 and Stryker personnel began visiting the facilities to make corrections.

Root Cause

Other

Distribution Pattern

California, Georgia, Indiana, Iowa, Michigan, Ohio and Pennsylvania.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K950889ADEL 5000Stryker Corp. · 1995-10-16

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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