Table, obstetrical, ac-powered (and accessories): medical device reports filed with FDA

4,666 reports carry this product code, 1992–2026; 18 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

4,666
reports with this product code: 0% of all MAUDE reports; 10
reports, 12 months to August 2026: 21 in the 12 months before; 98.4%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code HDD is FDA's classification for "Table, obstetrical, ac-powered (and accessories)" (obstetrics/Gynecology panel), a class 2 device. 4,666 medical device reports carry this product code, 0% of the MAUDE database, from July 1992 to July 2026.

10 reports arrived in the 12 months to August 2026, down 52% from 21 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (98.4%), injury (0.7%) and other (0.5%). 18 brand names with a page on this site carry this code; the brands table is ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Ld304 Maternity Bed	1,060	10	0%	98.3%
Affinity Bed	923	0	0%	98.9%
634 Affinity Bed 405	609	0	0%	99.8%
Affinity 4	534	0	0%	99.6%
Affinity 3	284	0	0%	95.8%
Affinity Three Birthing Bed	194	0	0%	100%
Gynnie Ob-Gyn Stretcher	90	11	0%	97.9%
Affinity 4 Birthing Bed	63	144	0%	98.4%
Stryker	2	5	1.3%	46.3%
4 Motor Advance Bed	1	0	0.4%	95.8%
Centra Bed	1	0	0.1%	98.9%
Hill-Rom	1	0	18.7%	31.1%
In Touch Zu	1	0	0.1%	96.1%
Secure Acute Care Bed	1	0	0%	98.6%
Skytron	1	1	0.9%	50.2%
Transtar Stretcher	1	5	0%	99.7%
Versacare Bed	1	0	0.2%	98.6%
Versacare Bed Versacare Frame	1	0	0.1%	99.2%

Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Hill-Rom Ritter	1,807	38.7%
Hill-Rom	1,434	30.7%
Stryker Medical	621	13.3%
Stryker Medical-Kalamazoo	570	12.2%
Stryker Medical Div	134	2.9%
Stryker Medical Division	42	0.9%
Stryker	4	0.1%
Hill-Rom De Mexico S De Rl De Cv	1	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death0%2

Injury0.7%32

Malfunction98.4%4,592

Other0.5%24

Not given0.3%16

Who filed

Manufacturer report99.3%4,633

Voluntary report0.3%13

User facility report0%0

Distributor report0%0

Not given0.4%20

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Device slipped	1,341	28.7%
Unintended system motionthe device moved when it should not have	830	17.8%
Sticking	538	11.5%
Breakthe device broke	345	7.4%
Unintended head motion	310	6.6%
Locking mechanism failure	307	6.6%
Loose	235	5%
Device operates differently than expectedthe device behaved unexpectedly	211	4.5%
Device inoperablethe device could not be used	155	3.3%
Mechanical problema mechanical problem	115	2.5%
Detachment of device component	89	1.9%
Grounding malfunction	86	1.8%
Component missing	79	1.7%
Drift	58	1.2%
Component falling	53	1.1%
Device alarm system	53	1.1%
Bent	46	1%
Crackthe device cracked	46	1%
Self-activation or keying	42	0.9%
Scratched material	41	0.9%

Questions about table, obstetrical, ac-powered (and accessories) reports

What is product code HDD?

FDA's classification code for "Table, obstetrical, ac-powered (and accessories)", class 2, reviewed by the obstetrics/Gynecology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

4,666 reports through August 2026, 10 of them in the latest 12 months.

Which brands appear most often?

Ld304 Maternity Bed (1,060), Affinity Bed (923), 634 Affinity Bed 405 (609), Affinity 4 (534) and Affinity 3 (284). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." Brands differ in how many are in use, how long they have been sold and how reports are collected.

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.