Boston Scientific Corporation AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders. Inflatable Penile Prosthesis Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders. Inflatable Penile Prosthesis
Brand
Boston Scientific Corporation
Lot Codes / Batch Numbers
visit: www.bostonscientific.com/lookup
Products Sold
UPNs 72404310 72404280 72404281 72404282 72404282-10 72404283 72404283-12 72404284 72404284-14 72404285 72404286 72404287 72404288 72404289 72404300 72404301 72404302 72404302-10 72404303 72404303-12 72404305 72404306 72404307 72404308 72404209 72404260 72404261 72404262 72404263 72404264 72404265 72404266 72404267 72404268 72404269 72404230 72404231 72404232 72404232-10 72404233 72404233-12 72404234 72404234-14 72404235 72404236 72404237 72404238 72404239 72404250 72404251 72404252 72404252-10 72404253 72404253-12 72404255 72404256 72404257 72404258 To determine if a UPN/serial number is impacted, visit: www.bostonscientific.com/lookup
Boston Scientific Corporation is recalling AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS due to The recalling firm has observed an increase in complaints of problems encountered during the initial activation of the device in which the patient and. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The recalling firm has observed an increase in complaints of problems encountered during the initial activation of the device in which the patient and/or the physician is unable or has difficulty activating the pump in order to achieve cylinder inflation.
Recommended Action
Per FDA guidance
On September 24, 2020, the firm issued Urgent Medical Device Removal letters to affected customers. Customers were instructed to do the following: 1. If you have affected inventory, immediately discontinue use of and segregate recalled product in a secure location for return to BSC. 2. Complete and return your response form via email or fax immediately. 3. Customers with affected inventory will receive an RGA# after emailing/faxing their form. Please wait to return any product until you receive the RGA#. 4. Return the recalled product to Boston Scientific Corporation.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026