Data Foundry

Medical device recalls 2024

Invacare Homecare Series Bed and Invacare G-Series Beds Containing… — Class II medical device recall Z-1251-2024

Ongoing recall by Invacare Corporation, reported 2024-03-13, distributed nationwide. Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld fa

Recall numberZ-1251-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmInvacare Corporation, Elyria, OH, United States
Recall initiated2024-01-22
Classified2024-03-04
Reported by FDA2024-03-13
DistributedNationwide (US)
Quantity8,117 units
Serial numbers23HX000067, 23HX000068, 23HX000069, 23HX000070, 23HX000071, 23HX000072, 23HX000073, 23HX000074, 23HX000075, 23HX000076, 23HX000077, 23HX000078, 23HX000079, 23HX000080, 23HX000081, 23HX000082, 23HX000083, 23HX000084, 23HX000085, 23HX000086, 23HX000087, 23HX000088, 23HX000089, 23HX000090, 23HX000091 and 475 more
Model numbers5000IVC, 5490IVC, 5490LOW, BAR5000IVC, BAR5490IVC, G50, G53, G54

Product

Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW

Reason for recall

Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1251-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.