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U.S. Department of Health and Human Services

Class 2 Device Recall Ultrasite Horizon Pump IV Set

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  Class 2 Device Recall Ultrasite Horizon Pump IV Set see related information
Date Initiated by Firm April 18, 2007
Date Posted May 31, 2007
Recall Status1 Terminated 3 on April 22, 2008
Recall Number Z-0818-2007
Recall Event ID 37856
510(K)Number K955585  K904518  
Product Classification IV Set - Product Code FPA
Product Ultrasite Horizon Pump IV Set. The product is shipped in cases containing 24 sets.
Code Information Lot numbers: 60883411 exp 9/09, 60886994 exp 9/09, 60883415 exp 9/09, 60883413 exp 9/09, 60883414 exp 9/09, 60883412 exp 9/09, 60883411 exp 9/09, 60883409 exp 9/09, 60883408 exp 9/09, 60883406 exp 9/09, 60883403 exp 9/09, 60884052 exp 9/09, 60884051 exp 9/09, 60883404 exp 9/09, 60883401 exp 8/09, 60883402 exp 8/09, 60883400 exp 8/09, 60883399 exp 8/09, 60883396 exp 8/09, 60883397 exp 8/09, 60883398 exp 8/09, 60880087 exp 8/09, 60880088 exp 8/09, 60880086 exp 8/09, 60880085 exp 8/09, 60880084 exp 8/09, 60880083 exp 8/09, 60880082 exp 8/09, 60880081 exp 8/09, 60880080 exp 8/09, 60880079 exp 8/09, 60880077 exp 8/09, 60880076 exp 8/09, 60880078 exp 8/09, 60880075 exp 8/09, 60880073 exp 8/09, 60880074 exp 8/09, 60875352 exp 7/09, 60875353 exp 7/09,60875350 exp 7/09, 60875348 exp 7/09, 60875349 exp 7/09, 60875347 exp 7/09, 60876056 exp 7/09, 60875345 exp 7/09, 60875346 exp 7/09, 60875344 exp 7/09, 60875343 exp 7/09, 60875342 exp 7/09, 60873263 exp 7/09, 60873262 exp 7/09, 60873260 exp 7/09, 60873261 exp 7/09, 60871825 exp 6/09, 60871439 exp 6/09, 60871824 exp 6/09, 60871823 exp 6/09, 60871438 exp 6/09, 60871437 exp 6/09, 60871436 exp 6/09, 60871435 exp 6/09, 60871434 exp 6/09, 60871433 exp 6/09, 60871431 exp 6/09, 60871432 exp 6/09, 60871430 exp 6/09, 60878152 exp 6/09, 60871429 exp 6/09, 60869484 exp 6/09, 60869482 exp 6/09, 60869479 exp 6/09, 60861428 exp 6/09, 60869467 exp 6/09, 60869466 exp 6/09, 60861993 exp 5/09, 60861995 exp 5/09, 60861996 exp 5/09, 00VL861992 exp 5/09, 00VL861991 exp 5/09, 00VL861990 exp 5/09, 60872855 exp 5/09, 60861985 exp 4/09, 60872856 exp 5/09, 60872854 exp 5/09, 60861989 exp 5/09 60861987 exp 5/09, 60859835 exp 5/09, 60861986 exp 5/09, 60859834 exp 5/09, 60859832 exp 5/09, 60859831 exp 5/09, 60859830 exp 5/09, 60872648 exp 5/09, 60872649 exp 5/09, 60859829 exp 5/09, 60880072 exp 8/09, 60880071 exp 8/09, 60880070 exp 8/09, 60880069 exp 7/09, 60875361 exp 7/09, 60875359 exp 7/09, 60875360 exp 7/09, 60875358 exp 7/09, 60875357 exp 7/09, 60875354 exp 7/09, 60875351 exp 7/09, 60869478 exp 6/09, 60869480 exp 6/09, 60869477 exp 6/09, 60869474 exp 6/09, 60869472 exp 6/09, 60869475 exp 6/09, 60872863 exp 6/09, 60869473 exp 6/09, 60869471 exp 6/09, 60869470 exp 6/09, 60869468 exp 6/09, 60883303 exp 9/09, 60883302 exp 9/09, 60883300 exp 9/09, 60883296 exp 9/09, 60892342 exp 9/09, 60892341 exp 9/09, 60892340 exp 8/09, 60894050 exp 8/09, 60892339 exp 8/09, 60894049 exp 8/09, 60883293 exp 8/09, 60883294 exp 8/09, 60880023 exp 8/09, 60880022 exp 8/09, 60891081 exp 8/09, 60891082 exp 8/09, 60891080 exp 8/09, 60880021 exp 8/09, 60878211 exp 8/09, 60878210 exp 8/09, 60889215 exp 8/09, 60878209 exp 8/09, 60878207 exp 8/09, 60878206 exp 8/09, 60888274 exp 7/09, 60878205 exp 7/09, 60878201 exp 7/09, 60886694 exp 7/09, 60886695 exp 7/09, 60878200 exp 7/09, 60875237 exp 7/09, 60875236 exp 7/09, 60875234 exp 7/09, 60875235 exp 7/09, 60883723 exp 7/09, 60873265 exp 7/09, 60875233 exp 7/09, 60873264 exp 7/09, 60869494 exp 6/09, 60869495 exp 6/09, 60869493 exp 6/09, 60882489 exp 6/09, 60869491 exp 6/09, 60869489 exp 6/09, 60869488 exp 6/09, 60862067 exp 6/09, 60877549 exp 6/09, 60862066 exp 6/09, 60862065 exp 6/09, 60861761 exp 6/09, 60861760 exp 6/09, 60870771 exp 6/09, 60861759 exp 6/09, 60862063 exp 6/09, 60862064 exp 6/09, 60861758 exp 6/09, and 60861757 exp 5/09.
Recalling Firm/
Manufacturer		 B. Braun Medical, Inc.
901 Marcon Boulevard
Allentown PA 18109-9512
For Additional Information Contact Kimberly Paris
610-266-0500
Manufacturer Reason
for Recall		 Secondary infusion backs up into primary container.
FDA Determined
Cause 2		 Other
Action The recalling firm issued Product Removal Notices on 4/20/07 via certified priority mail. The notice informed the customer of the problem and the need to return the product.
Quantity in Commerce 2.5 million for all products
Distribution Nationwide and Canada.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = FPA and Original Applicant = B. BRAUN MEDICAL, INC.
510(K)s with Product Code = FPA and Original Applicant = KENDALL MCGAW LABORATORIES, INC.
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