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FDA Medical Device Recalls (openFDA)

Fetzer Medical GmbH & Co. KG: 12002 / Boss Instruments Ltd. Wrigley Obstetric Forceps, 11" (28cm), Item No./Product Code 46-5004 Fetzer Medical Obstetrical Forceps is a hand-held instruments intended to assist the birth of a foetus during difficult vaginal births through grasping the foetal head in order to facilitate its passage through the birth canal. The instruments are only used for female population. The product is non-powder, non-liquid, non-tablet, capsule or other.

Recall number
Z-0756-2019
Recalling firm
Fetzer Medical GmbH & Co. KG
Product
12002 / Boss Instruments Ltd. Wrigley Obstetric Forceps, 11" (28cm), Item No./Product Code 46-5004 Fetzer Medical Obstetrical Forceps is a hand-held instruments intended to assist the birth of a foetus during difficult vaginal births through grasping the foetal head in order to facilitate its passage through the birth canal. The instruments are only used for female population. The product is non-powder, non-liquid, non-tablet, capsule or other.
Status
Terminated
Initiated
2018-12-28
Posted
2019-01-18
Terminated
2020-09-17
Reason
The firm had a report of doctors being unable to pull the obstetric forceps apart.
Root cause
Device Design
Action
The recalling firm, Fetzer Medical, notified its consignees by email with an "URGENT: VOLUNTARY PRODUCT RECALL" letter dated 12/27/2018 on 12/28/20018. The letter described the product, problem and actions to be taken. The consignees were instructed to do the following: 1. Examine your inventory immediately to determine if you have product subject to this action on hand and quarantine such product(s). 2. Remove the product subject to this voluntary recall and communicate the issue to relevant operating room or materials management personnel, or anyone else in your facility who needs to be informed. 3. If any product subject to this action has been forwarded to another facility, contact that facility to arrange return. 4. Complete the Reply Form (RF) (Attachment) confirming receipt of this notice and fax this form to Fetzer Medical GmbH & Co. KG, 49 (0) 7462-94799-100 or e-mail the form to dkaufmann@fetzermed.com, without delay, even if you do not have product subject to this recall to return. 5. Keep this notice visibly posted for awareness until all products subject to this recall have been returned to Fetzer Medical. While processing your returns, please maintain a copy of this notice with the product subject to this action and keep a copy for your records. 6. Customers are required to return all affected lots of the affected products that are in their inventory immediately. A replacement of the affected products is not possible, as Fetzer Medical has stopped production of these items. To receive a credit note, please contact Fetzer Medical via contact information below. Only requests submitted before February 1st, 2019 will be considered. 7. To return unused Obstetrical Forceps lots subject to this action, photocopy the completed RF, place it in the box with the product, and send it back to Fetzer Medical. If you have any further questions related to this notice or if you need any additional communications, please contact Fetzer Medical at + 49 (0) 74
Quantity
10 units
Distribution
US Distribution to states of: IL and VA.
Lot, serial or model codes
Lot Number 13300828
510(k) numbers
["K172661"]
PMA numbers
not on file
Product code
HDA
Firm FEI
3007648354
Firm city
Tuttlingen
Firm state
not on file
Firm country
Germany

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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