Affinity¿ Four Birthing Bed — Class II medical device recall Z-2562-2014

Terminated recall by Hill-Rom, Inc., reported 2014-09-10, distributed nationwide. The attachment latch mechanism can become bent depending on user handling. Latch mechanism bending could lead

Recall number	`Z-2562-2014`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Hill-Rom, Inc., Batesville, IN, United States
Recall initiated	2014-06-26
Classified	2014-09-01
Reported by FDA	2014-09-10
Terminated	2017-07-14
Distributed	Nationwide (US)
Countries outside the US	AE, AR, AT, AU, AW, BE, BG, BH, BM, BR, BS, BZ, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DO, EG, ES, FI, FR, GB, GR, GY, HK, HR, HU, ID, IE, IL, IN, IQ, IT, JO, JP, KE, KR, KW, KY, LB, MA, MX, MY, NG, NL, NO, NZ, OM, PH, PK, PL, PT, QA, RO, RS, SA, SE, SG, SI, TH, TN, TR, TT, TW, VE, VN, ZA
Quantity	13,000 units
Model numbers	`P3700B`, `P3700C`, `P3700D`, `P3700E`

Product

Affinity¿ Four Birthing Bed, Product Usage: Product is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market.

Reason for recall

The attachment latch mechanism can become bent depending on user handling. Latch mechanism bending could lead to improper engagement of the foot section and this could result in injury to the user due to a fall.

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-2562-2014. 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.