Recalls affecting Oregon

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

Recall #:

H-0768-2026

Lot/product code:

Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026

Recalling firm:

Dakota Honey Company

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

Recall #:

H-0770-2026

Lot/product code:

Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026

Recalling firm:

Dakota Honey Company

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

Recall #:

H-0769-2026

Lot/product code:

Honey does not have any code on container. 1. 4 oz spun honey purchased from December 19, 2025 to April 3, 2026 2. 12 oz spun honey purchased from February 25, 2026 to April 3, 2026

Recalling firm:

Dakota Honey Company

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

Recall #:

H-0772-2026

Lot/product code:

Honey does not have any code on container. 4 oz spun honey Flights purchased from December 19, 2025 to April 3, 2026

Recalling firm:

Dakota Honey Company

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

Recall #:

98707

Lot/product code:

Part Number: 150450205. UDI-DI: 10603295533160. Lot Number: 1006444. Expiration Date: 10/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98707

Lot/product code:

Part Number: 150450207. UDI-DI: 10603295533177. Lot Number: 1007046. Expiration Date: 10/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98704

Lot/product code:

Lot Code: 08717213024205

Recalling firm:

Elekta, Inc.

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

Recall #:

98707

Lot/product code:

Part Number: 150450104. UDI-DI: 10603295533115. Lot Number: 1007844. Expiration Date: 11/30/2035

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98707

Lot/product code:

Part Number: 150450108. UDI-DI: 10603295543022. Lot Number: AF1006441. Expiration Date: 12/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98707

Lot/product code:

Part Number: 150450204. UDI-DI: 10603295533153. Lot Number: 1005229. Expiration Date: 10/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98707

Lot/product code:

Part Number: 150450105. UDI-DI: 10603295533122. Lot Number: AF1007829. Expiration Date: 12/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98707

Lot/product code:

Part Number: 150450107. UDI-DI: 10603295533139. Lot Number: 1006440. Expiration Date: 11/30/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98704

Lot/product code:

Lot Code: 08717213055001, 08717213055018, 08717213055025, 08717213055049, 08717213055056, 08717213055063, 08717213055087, 08717213055094, 08717213055100, 08717213055117, 08717213055131

Recalling firm:

Elekta, Inc.

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

Recall #:

98707

Lot/product code:

Part Number: 150450203. UDI-DI: 10603295533146. Lot Number: 1007537. Expiration Date: 10/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98704

Lot/product code:

Lot Code: 08717213056039, 08717213056053, 08717213056077, 08717213056091, 08717213056398, 08717213056411, 08717213056435, 08717213056459, 08717213056473, 08717213056497, 08717213056510,08717213056534, 08717213056558, 08717213056572, 08717213056596, 08717213056619, 08717213056633, 08717213056657

Recalling firm:

Elekta, Inc.

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

Recall #:

98707

Lot/product code:

Part Number: 150450208. UDI-DI: 10603295543039. Lot Numbers: AF1008441, AF1008028. Expiration Date: 12/31/2035.

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

98773

Lot/product code:

Model/Catalog Number: 409-375 UDI code: (01)00844505000772(10)122927(17)310301 Lot Number: 122927

Recalling firm:

Grace Medical, Inc.

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

Recall #:

98773

Lot/product code:

Model/Catalog Number: 409-375 UDI code: (01)00844505000772(10)122927(17)310301 Lot Number: 122927

Recalling firm:

Grace Medical, Inc.

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

H-1263-2026

Lot/product code:

Sold between July - December 2025

Recalling firm:

ZMB Enterprises

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

Recall #:

98739

Lot/product code:

UDI: 08806141303077/ Lot: 241023, 250415, 250509, 250617, 250905

Recalling firm:

DFI Co., Ltd.

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

Recall #:

98682

Lot/product code:

UDI-DI 00827002473089 Lots 16858459 16869145 16857138 16763324 16750208 16752733 16821053 16713191

Recalling firm:

Cook Incorporated

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

Recall #:

D-0497-2026

Lot/product code:

Lot # J5E226, J5E227, J5E228, J5E229, J5E230, J5E231, J5E232, J5E233, J5E238, J5E239, Exp Date: 30Apr2028, Lot # J5E240, J5E241, J5E242, J5E243, J5E244, J5E245, J5E247, J5E248, Exp Date: 30Apr2028, Lot # J5H151, J5H152, J5H153, J5H154, J5H155, Exp Date: 31 May2028.

Recalling firm:

B BRAUN MEDICAL INC

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

Recall #:

98682

Lot/product code:

G31213 UDI-DI 00827002312135 Lot 16805456 G31214 UDI-DI 00827002312142 Lots 16886459 16874181 16855513 16867505 16815763 16796665 16802282 16766437 16734169 16695772 G31216 UDI-DI 00827002312166 Lots 16886460 16891299 16912494 16831676 16836358 16836359 16836360 16864534 16864652 16881655 16882508 16912493 16872559 16878260 16824312 16831675 16874182 16855514 16868889 16859732 16858079 16878261 16806270 16804619 16805454 16804399 16815762 16803920 16803921 16802096 16802097 16814369 16814370 16806333 16804620 16831528 16822289 16822290 16782945 16782946 16795733 16796300 16779437 16795734 16800424 16802632 16824313 16764526 16763024 16800730 16802633 16802133 16800731 16821105 16824314 16711110 16717839 16730326 16720153 16736740 16739291 16693653 16690051 16673569 16680240 16704378 G31220 UDI-DI 00827002312203 Lots 16881657 16872241 16827163 16852999 16805455 16804400 16802132 16779438 16730325 16739292 16700199 16690050 16661312 16674400 G31221 UDI-DI 00827002312210 Lots 16839296 16879977 16814371 16821104

Recalling firm:

Cook Incorporated

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

Recall #:

D-0495-2026

Lot/product code:

Lot # J5H165, Exp Date: 31 May2028; Lot # J5E237, Exp Date: 30APR2028.

Recalling firm:

B BRAUN MEDICAL INC

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

Recall #:

98637

Lot/product code:

All Lot Numbers/UDI: 00884450816509

Recalling firm:

Merit Medical Systems, Inc.