Home/Recalls/FDA-Z-1427-2026
FDA DevicesClass II

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 1...

Published: February 25, 2026Recall ID: Z-1427-2026Category: devicesCountry: US

Reason for Recall / Hazard

Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.

Product Description & Identification

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195134 MP2001 - MOLLI 2 Wand UDI (GTIN): 00850024195141 MP2015A - MOLLI OncoPen UDI (GTIN): 00850024195219 MT2001 - MOLLI 2 Tablet UDI (GTIN): 00850024195158 The MOLLI Marker is intended to be placed percutaneously in soft tissue to temporarily mark a surgical site intended for surgical removal. the MOLLI Marker is located and surgically removed with the target tissue.

Affected Products

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195134 MP2001 - MOLLI 2 Wand UDI (GTIN): 00850024195141 MP2015A - MOLLI OncoPen UDI (GTIN): 00850024195219 MT2001 - MOLLI 2 Tablet UDI (GTIN): 00850024195158 The MOLLI Marker is intended to be placed percutaneously in soft tissue to temporarily mark a surgical site intended for surgical removal. the MOLLI Marker is located and surgically removed with the target tissue.

Additional Source Details

FieldValue
CitySan Jose
StateCA
Event id98295
Address 15900 Optical Ct
Code infoCatalog Number: MM1000 (Pack of 10) UDI (GTIN): 00850024195028 Serial Numbers: 23-0350 24-0118 24-0289 24-0290 24-0291 24-0472 24-0473 24-0474 24-0534 24-0535 24-0536 24-0658 24-0660 24-0697 25-0020 25-0021 25-0022 25-0160 25-0161 25-0162 25-0353 25-0354 25-1057 25-1058 25-1060 25-1087 23-0003 23-0046 23-0057 23-0062 23-0125 23-0126 23-0129 23-0176 23-0177 23-0179 23-0413 23-0414 24-0413 Catalog Number: MS-00009 (Pack of 10) UDI (GTIN):00850024195134 Serial Numbers: 22-0130 23-0022 23-0130 23-0178 24-0035 24-0117 24-0225 24-0235 24-0236 24-0659 24-0696 24-0719 25-0251 25-0252 Catalog Number: MP2001 UDI (GTIN): 00850024195141 Serial Numbers: 16 18 29 30 32 43 49 54 60 62 66 77 80 81 84 85 92 93 100 101 114 115 138 155 158 160 163 164 174 180 181 182 184 186 190 199 202 203 216 217 218 220 221 222 225 226 227 228 229 230 231 232 234 235 236 237 238 239 240 241 242 243 244 245 246 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 273 274 275... [TRUNCATED]
Postal code95138-1400
Report date20260225
Product typeDevices
Product quantity5,864
Reason for recallDue to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260121
Initial firm notificationLetter
Center classification date20260217

Overview

  • Recalling FirmStryker Corporation
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide - U.S. Nationwide distribution including in the states of AL, AK, AZ, AR, CA, CO, CT, DC, FL, GA, HI ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WV, WI, and WY. The countries of Canada, Singapore, Panama, Jamaica, and Cayman Islands.
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