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Lot Number 7RSL021
Device Problem Microbial Contamination of Device (2303)
Patient Problems Pain (1994); Swelling (2091); No Code Available (3191)
Event Date 01/01/2017
Event Type  Injury  
Event Description
Increased pain [pain aggravated]. Increased swelling [swelling]. Device malfunction [device malfunction]. Case narrative: case was initially submitted via sanofi legacy database and is now being re-distributed to fda at their request. This unsolicited case was received from united states on (b)(6) 2018 from other non-healthcare professional via regulatory authority: usa-fda. This case involves a female patient of unknown age who received treatment with synvisc one and had increased pain and increased swelling (both after unknown latency). Also, device malfunction was identified for the reported lot number. No relevant medical history, past drugs, concomitant medications and concurrent conditions were reported. On unknown date in 2017, patient received treatment with intra-articular synvisc one injection (dose, frequency, indication: not reported; batch/lot number: 7rsl021; expiry date: not reported). On unknown date in 2017, (post injection), after unknown latency, patient had 3 days increased pain and swelling. Patient was no longer having symptoms. Event stopped after abate or dose reduced. Corrective treatment: not reported for all the events. Outcome: recovered/ resolved for all the events. An investigation was initiated as a result of an unexpected increase in the number of labelled adverse events received from the us market for synvisc one, lot 7rsl021. The product met all release testing at time of manufacture in june 2017. Retain samples were retested due to the unexpected increase in adverse events. Higher than expected endotoxin results were obtained. In addition, the presence of microbial contamination was also confirmed. The cause of these events was under investigation. Once this investigation is completed, corrective and preventive actions would be implemented. Seriousness criteria: important medical event for all the events. Pharmacovigilance comments: sanofi company comment for dated 27-feb-2018: this case concerns a patient who has received synvisc one injection from the recalled lot and later had increased pain and swelling. The concerned lot number has been identified to have malfunction by the company. Therefore, the causal relationship of the events to the products cannot be excluded.
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Type of DeviceMOZ
Manufacturer (Section D)
1125 pleasantview terrace
ridgefield 07657
Manufacturer (Section G)
1125 pleasantview terrace
ridgefield 07657
Manufacturer Contact
heather schiappacasse
55 corporate drive, ms 55b-220
bridgewater 08807
MDR Report Key7327111
MDR Text Key204575975
Report Number2246315-2018-00368
Device Sequence Number1
Product Code MOZ
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Remedial Action Recall
Type of Report Initial
Report Date 08/26/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/09/2018
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator
Device Lot Number7RSL021
Was Device Available for Evaluation? No
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

Patient Treatment Data
Date Received: 03/09/2018 Patient Sequence Number: 1