MAGNETOM Aera magnetic resonance diagnostic devices recall
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Why was MAGNETOM Aera magnetic resonance diagnostic devices recalled?
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial # 41878 52409 142129 141526 42163 152267 141686 42436 42160 142132 41953 141226 141862 141521 42225 52171 41980 41051 152232 42247 141462 52299 52338 42416 141199 141557 142109 141054 152249 42020 41794 142147 152217 141951 42458 141638 42087 142010 42326 142009 142124 141676 42290 52229 42298 142130 141561 141973 42530 141141 41951 42236 152215 42267 42364 141305 42372 142122 42083 142142 42217 52195 152175 41945 141712 42256 42310 41780 42422 141963 42534 52350 52249 42412 42413 52397 41862 141786 42420 52221 52304 42306 141513 142024 141016 42495 142120 41906 52267 141589 42249 42158 41897 52321 42303 141056 42353 42330 41778 141275 141109 142107 42381 42339 41777 152234 52190 141201 42566 141677 41782 42254 42214 52192 141314 141585 42248 42295 42517 141072 42417 141439 141975 142104 41941 41813 141260 42533 141386 52157 141154 141135 142128 141121 142077 141242 142074 141253 141043 141221 42635 42507 141025
- Product
- MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 143
- Distribution
- AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
- Recall date
- August 28, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)