Data Foundry

Medical device recalls 2019

Posey Connected Twice-As-Tough Cuffs — Class II medical device recall Z-0194-2020

Terminated recall by TIDI PRODUCTS, reported 2019-11-06, distributed in AK, AR, CA, CT, FL, GA, IA, IL…. Not meeting design specifications.

Recall numberZ-0194-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTIDI PRODUCTS, Lake Forest, IL, United States
Recall initiated2019-04-12
Classified2019-10-25
Reported by FDA2019-11-06
Terminated2020-07-22
DistributedAK, AR, CA, CT, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MN, MO, MS, MT, NC, NH, NJ, NM, NY, PA, SC, TN, TX, UT, VA, VT, WI, WV
Countries outside the USCA, FR, NL
Lot numbers059T038, 122T083, 7038T010, 7044T051, 7061T050, 7088T028, 7089T002, 7090T054, 7100T047, 7103T054, 7109T007, 7112T001, 7114T090, 7114T091, 7151T004, 7154T006, 7156T124, 7163T046, 7165T087, 7178T035, 7181T003, 7185T008, 7185T014, 7186T103, 7192T034, 7194T051, 7200T090, 7250T051, 7263T007, 7271T210, 7284T006, 7284T105, 7291T094, 7313T054, 7317T014, 7340T102, 7347T110, 7354T115, 7355T062, 7361T073 and 47 more
Model numbers2796, 2797

Product

Posey Connected Twice-As-Tough Cuffs

Reason for recall

Not meeting design specifications.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0194-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.