Recalls affecting Oregon

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

H-0401-2026

Lot/product code:

Product Codes: 231874 4D20 & 231874 4D21 Best By: 4/19/2026 & 4/20/2026

Recalling firm:

AZ Gems, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

97546

Lot/product code:

Catalog Number: 1115-00 Software Versions: UDI-DI code for Hardware: 10885403518348 UDI-DI code for Software: 10885403520341 System Versions 1.6.1 - 1.11.0 Server Application Versions ES 4.13 - 5.8.X

Recalling firm:

CareFusion 303, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98097

Lot/product code:

version 2.0.2465 and 2.0.2683 UDI-DI (GTIN) 00763000520083 Affected product is the software. Implanted Vanta Neurostimulator devices are not affected.

Recalling firm:

Medtronic Neuromodulation

FDA has not published a risk classification for this recall yet.

Recall #:

98149

Lot/product code:

1) GTIN 08714729796527, Batch Number 37370117, exp. 3-Sept-28; 2) GTIN 08714729796756, Batch Number 37416646, exp. 9-Sept-28

Recalling firm:

Boston Scientific Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 781342; UDI-DI: 00884838055339; Serial Numbers: 71607, 85216, 71087, 71619, 71462, 71002, 71885, 71841, 71378, 71269, 85126, 71279, 71088, 71185, 71532, 71344, 71756, 71336, 71459. (2) Product Code (REF): 781377; UDI-DI: 00884838009813; Serial Numbers: 42305, 42299, 42036, 42376, 42321.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98238

Lot/product code:

N/A

Recalling firm:

Philips Healthcare (Suzhou) Co., Ltd.

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. Product Code (REF): 782108. UDI-DI: 00884838098343. Serial Numbers: 48669.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 781341; UDI-DI: 00884838055322; Serial Numbers: 70311, 84560, 84403, 84467, 84462, 70042, 84433. (2) Product Code (REF): 781396; UDI-DI: 00884838009820; Serial Numbers: 41356, 41354, 41370.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 781357; UDI-DI: 00884838088108; Serial Numbers: 46002. (2) Product Code (REF): 782106; UDI-DI: 00884838098329; Serial Numbers: 46243, 46292. (3) Product Code (REF): 782137; UDI-DI: 00884838108615; Serial Numbers: 64034, 64045.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. Product Code (REF): 782145. UDI-DI: 00884838108684. Serial Numbers: 17385.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 782148. UDI-DI: 00884838108714. Serial Numbers: 70769, 70983. (2) Product Code (REF): 782116. UDI-DI: 00884838099722. Serial Number: 84741.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. Product Code (REF): 782143. UDI-DI: 00884838108660. Serial Numbers: 42225.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. Product Code (REF): 781270. UDI-DI: 00884838095083. Serial Numbers: 24066, 38113, 17356.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. Product Code (REF): 782130. UDI-DI: 00884838104402. Serial Numbers: 42030, 85644, 42163, 42151, 45236, 85643.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. Product Code (REF): 781271. UDI-DI: 00884838068452. Serial Numbers: 78017, 78112, 78217, 78123, 78260, 78239.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 782120; UDI-DI: 00884838104112; Serial Numbers: 65019, 65060, 65066, 65065, 65051, 65038, 65005. (2) Product Code (REF): 782153; UDI-DI: 00884838112858; Serial Numbers: 68010, 68017.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 781358; UDI-DI: 00884838088115; Serial Numbers: 45414, 45245, 45090, 45049, 45034, 45250, 45075, 45290, 45320, 45011, 45191, 45277, 45278, 45028, 45147. (2) Product Code (REF): 782107; UDI-DI: 00884838098336; Serial Numbers: 62031, 45533, 62051, 62182, 62024, 62047, 62048, 62052, 45519, 62181, 62081, 62153, 62088, 45589, 62073. (3) Product Code (REF): 782136; UDI-DI: 00884838108608; Serial Numbers: 28503.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98111

Lot/product code:

MR systems with SW version R11.1 and R12.1. (1) Product Code (REF): 781356; UDI-DI: 00884838090040; Serial Numbers: 47206, 47038, 47068, 47260, 47294, 47029, 47189. (2) Product Code (REF): 782109; UDI-DI: 00884838098350; Serial Numbers: 47849, 47634, 47534, 47726, 47760, 47706, 47789, 47642, 47681, 47761, 47771, 47767, 47862. (3) Product Code (REF): 782138; UDI-DI: 00884838108622; Serial Numbers: 49057.

Recalling firm:

Philips North America

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815609400 ; UDI-DI (01)00887868144516(17)340818(10)66717605 ; Lot Number 66717605 Model No 815609400 ; UDI-DI (01)00887868144516(17)340826(10)66892904 ; Lot Number 66892904 Model No 815609400 ; UDI-DI (01)00887868144516(17)341024(10)67031552 ; Lot Number 67031552

Recalling firm:

Zimmer, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815609420 ; UDI-DI (01)00887868144523(17)340818(10)66717606 ; Lot Number 66717606 Model No 815609420 ; UDI-DI (01)00887868144523(17)340913(10)66892905 ; Lot Number 66892905

Recalling firm:

Zimmer, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815509380 ; UDI-DI (01)00887868143557(17)340822(10)66717554 ; Lot Number 66717554 Model No 815509380 ; UDI-DI (01)00887868143557(17)340822(10)66884564 ; Lot Number 66884564 Model No 815509380 ; UDI-DI (01)00887868143557(17)350421(10)67042197 ; Lot Number 67042197

Recalling firm:

Zimmer, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815509300 ; UDI-DI (01)00887868143519(17)340823(10)66717550 ; Lot Number 66717550

Recalling firm:

Zimmer, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815509400 ; UDI-DI (01)00887868143564(17)340821(10)66717555 ; Lot Number 66717555 Model No 815509400 ; UDI-DI (01)00887868143564(17)340822(10)66884565 ; Lot Number 66884565 Model No 815509400 ; UDI-DI (01)00887868143564(17)350801(10)67379212 ; Lot Number 67379212

Recalling firm:

Zimmer, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815509360 ; UDI-DI (01)00887868143540(17)340917(10)66717553 ; Lot Number 66717553 Model No 815509360 ; UDI-DI (01)00887868143540(17)340823(10)66884563 ; Lot Number 66884563

Recalling firm:

Zimmer, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98069

Lot/product code:

Lot Code: Model No 815509340 ; UDI-DI (01)00887868143533(17)340822(10)66717552 ; Lot Number 66717552 Model No 815509340 ; UDI-DI (01)00887868143533(17)340826(10)66884562 ; Lot Number 66884562

Recalling firm:

Zimmer, Inc.