Recalls affecting Illinois

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-0771-2026

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

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 #:

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 #:

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

Recalling firm:

DEPUY (IRELAND)

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

Recall #:

H-0767-2026

Lot/product code:

Lot, Best Before: 260201MA, 01FEB2027; 260202MA, 02FEB2027.

Recalling firm:

Wehah Farms

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 #:

98707

Lot/product code:

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

Recalling firm:

DEPUY (IRELAND)

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 #:

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: 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 #:

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.

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: 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 #:

98680

Lot/product code:

Siemens Material Number (SMN): 10736515; UDI-DI: 00809708121860; Lot numbers: 01-26024-70, 01-26026-70, 01-26028-70, 01-26030-70 (OUS only), 02-26027-80, 02-26028-80 (OUS only);

Recalling firm:

Siemens Healthcare Diagnostics Inc

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

Recall #:

98564

Lot/product code:

Lot Code: UDI: 00886874114216 FDA Medical Device Listing Number: D531324 See attachment Affected Product List UDI: 00886874114216 FDA Medical Device Listing Number: D295931 See attachment Affected Product List

Recalling firm:

Intuitive Surgical, Inc.

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

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

Recall #:

98741

Lot/product code:

Pack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088

Recalling firm:

Windstone Medical Packaging, Inc.

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

Recall #:

98739

Lot/product code:

UDI: 08806141303060/ Lot: BS032501, BS042502, BS062501, BS062502, BS082501

Recalling firm:

DFI Co., Ltd.

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

Recall #:

98739

Lot/product code:

UDI: 08806141303060/ Lot: 250305, 250415, 250509, 250625, 250905

Recalling firm:

DFI Co., Ltd.

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

Recall #:

98739

Lot/product code:

UDI: 08806141303497/ Lot: 241023, 250305, 250415, 250527, 250625, 250905

Recalling firm:

DFI Co., Ltd.