Z-0147-2011

Recalled chairs include the following: 2008 Model Numbers: 653N - Care Cliner, 654N - XL Care Cliner, 655N...

Name: Z-0147-2011 Recalled chairs include the following: 2008 Model Numbers: 653N - Care Cliner, 654N - XL Care Cliner, 655N...
Creator: Winco, Inc.
Published: 2010-09-07
License: https://open.fda.gov/license/

Champion Mfg, Inc. / initiated 2010-09-07 / Terminated / root cause: design

FDA source

Winco, Inc. began a recall of Recalled chairs include the following: 2008 Model Numbers: 653N - Care Cliner, 654N - XL Care Cliner, 655N - Drop Arm Care Cliner, 657N - XL Drop Arm Care... on 2010-09-07. The reason FDA records is "Winco Mfg., LLC, Ocala, Florida is recalling their Care Cliner. Due to malfunctioning axles which become lose from the caster assembly. This chair is a multi position recliner with a steel frame used primarily in...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0147-2011
Status: Terminated
Initiated: 2010-09-07
Posted: 2010-10-27
Terminated: 2011-05-20
Recalling firm: Champion Mfg, Inc.
Product: Recalled chairs include the following: 2008 Model Numbers: 653N - Care Cliner, 654N - XL Care Cliner, 655N - Drop Arm Care Cliner, 657N - XL Drop Arm Care Cliner, 690N - Elite Care Cliner, 691N - XL Elite Care Cliner, 694N - Dual Swing-Arm Elite Care Cliner, 695N - XL Dual Swing-Arm Elite Care Cliner. 2009 Model Numbers: 6530 - Care Cliner, 6540 - XL Care Cliner, 6550 - Drop Arm Care Cliner, 6570- XL Drop Arm Care Cliner, 6900 - Elite Care Cliner, 6910 - XL Elite Care Cliner, 6940 - Dual Swing-Arm Elite Care Cliner, 6950 - XL Dual Swing-Arm Elite Care Cliner.
Product code: INM Chair, With Casters
Reason for recall: Winco Mfg., LLC, Ocala, Florida is recalling their Care Cliner. Due to malfunctioning axles which become lose from the caster assembly. This chair is a multi position recliner with a steel frame used primarily in clinics, hospitals and treatment centers for recovery, dialysis, oncology, examination, infusion. Recalled chairs include the following: Care Cliner, XL Care Cliner, Drop Arm Care Cliner
Root cause tag: design
FDA root cause: Device Design
Action: Winco sent an Urgent Device Recall letter dated October 1, 2010, to all customers. The letter identified the product, the problem, and the action to be taken by the customer. Replacement parts were sent out to the consignees and customers were asked to dispose of the defective casters. Any consignee not reponding by November 15, 2010, would receive an additional letter. The firm placed a follow up phone call to the non responding consignees after two weeks. Customers were advised to call 800-237-3377 or email customer service at [email protected] with questions or concerns. For questions or concerns regarding this recall call 352-854-2929 x 110.
Quantity in commerce: 18,522 casters
Distribution: Worldwide Distribution - USA (all states except Vermont and Nebraska) and the countries of Belgium, Canada, Chile, Ireland, Kuwait, Netherlands, Saud Arabia, Singapore and United Arab Emirates.
Product codes and lots: Recalled chairs include the following Models : Recalled chairs include the following: 2008 Model Numbers: 653N - Care Cliner, 654N - XL Care Cliner, 655N - Drop Arm Care Cliner, 657N - XL Drop Arm Care Cliner, 690N - Elite Care Cliner, 691N - XL Elite Care Cliner, 694N - Dual Swing-Arm Elite Care Cliner, 695N - XL Dual Swing-Arm Elite Care Cliner. 2009 Model Numbers: 6530 - Care Cliner, 6540 - XL Care Cliner, 6550 - Drop Arm Care Cliner, 6570- XL Drop Arm Care Cliner, 6900 - Elite Care Cliner, 6910 - XL Elite Care Cliner, 6940 - Dual Swing-Arm Elite Care Cliner, 6950 - XL Dual Swing-Arm Elite Care Cliner. Recalled model numbers are as folows: 6530-02, 6530-03, 6530-03-TB, 6530-04, 6530-06, 6530-07, 6530-08, 6530-08-TB-00-PB, 6530-14, 6530-15, 6530-15-00-00-00-00-LC, 6530-15-00-00-PB, 6530-16, 6530-17, 6530-17-TB, 6530-25, 65302N, 65302NT, 6530-30, 6530-31, 6530-33, 6530-37-00-00-PB, 6530-39, 6530-39-00-00-PB, 65303N, 65303N, 65304N, 65304NH, 65304NHT, 65304NT, 6530-63, 6530-63-TB, 65306N, 65306NH, 65307N, 65307NT, 65308N, 65308NT, 65314N, 65314NH, 65314NT, 65315N, 65316N, 65317N, 65317NT, 65330N, 65333NT, 65337N, 65341N, 65344N, 65360N, 65361N, 65362N, 65362NT, 65363N, 65363NT, 6540-02, 6540-03, 6540-04, 6540-04-00-HM, 6540-06, 6540-07, 6540-08, 6540-14, 6540-16-TB, 6540-17, 6540-17-TB, 65402N, 65402NT, 6540-30-00-00-PB, 6540-37, 6540-39, 6540-39-00-00-PB, 65403N, 65403NT, 65404N, 65404NH, 65404NHT, 6540-60, 6540-63-TB, 65406N, 65406NH, 65407N, 65408N, 65414N, 65414NT, 65415N, 65416N, 65417N, 65417NT, 65430N, 65437N, 65441N, 65442N, 65461NH, 65462N, 65465N, 6550-02, 6550-03, 6550-03-00-HM, 6550-04, 6550-06, 6550-13, 6550-14, 6550-14-00-00-PB, 6550-14-00-HM, 6550-16, 6550-17, 65502N, 6550-30-00-HM, 6550-34-00-00-PB, 6550-37, 6550-39-00-HM, 65503N, 65503NH, 65504N, 65504NL, 65504NT, 65504NT-DART, 65506N, 65506NH, 65507N, 65507NH, 65508N, 65514N, 65514NH, 65514NL, 65514NW, 65515N, 65516N, 65516NH, 65516NT, 65517N, 65517NCE, 65517NH, 65517NHT, 65525N, 65527N, 65527NH, 65528NH, 65530NH, 65532N, 65532NH, 65533N, 65537N, 65539N, 65539NH, 65541NL, 65544NW, 65561NL, 65562NH, 65562NL, 65567N, 65567NH, 6570-02, 6570-03, 6570-03-00-HM, 6570-07, 6570-14, 6570-14-00-00-PB, 6570-14-00-HM, 6570-17, 6570-17-00-00-PB, 6570-17-00-00-PC, 6570-17-TB, 65702N, 65702NT, 6570-39-00-HM, 65703N, 65703NH, 6570-41, 65704N, 65704NT, 6570-62, 6570-63-TB, 65706N , 65706NH, 65707N, 65707NH, 65708N, 65708NT, 65714N, 65714NH, 65714NL, 65714NT, 65714NW, 65715N, 65716NH, 65717N, 65717NCE, 65717NH, 65725N, 65727NH, 65728NH, 65730N, 65730NH, 65732N, 65732NH, 65733N, 65737N, 65739N, 65739NH, 65741NH, 65741NL, 65761N, 65762N, 65762NH, 65762NL, 65763NH, 65766N, 65767NH, 6900-02, 6900-03, 6900-04, 6900-17, 69002N , 6900-30, 6900-39 , 69003N, 69003NH, 6900-41, 69004N, 6900-60, 6900-61, 6900-62, 6900-63, 6900-63-00-HM, 6900-63-TB, 69006N, 69007N, 69008N, 69008NH, 69014N, 69014NT, 69014NW, 69015N, 69016N, 69016NT, 69017N, 69017NH, 69026N, 69027N, 69028N, 69030N, 69030NH, 69031N, 69032N, 69033N, 69034N, 69037N, 69039N, 69041N, 69041NH, 69060N, 69062N, 69063N, 69063NH, 69063NT, 69065NT, 69066N, 69066NT, 69067N, 6910-03, 6910-06, 6910-17, 6910-32, 6910-33-00-HM, 6910-37-00-00-PB, 6910-37-TB, 6910-39, 69103N, 69104N, 6910-60, 6910-61, 6910-62, 6910-63, 69106N, 69107NT, 69114N, 69114NW, 69117N, 69117NH, 69117NT, 69127N, 69133N, 69133NT, 69134N, 69137N, 69162N, 69163N, 69167N, 6940-03, 6940-03-00-HT, 6940-04-TB-HT, 6940-06, 6940-06-TB-HM, 6940-07-TB, 6940-14, 6940-14-TB, 6940-15, 6940-15-00-HM, 6940-16, 6940-16-TB-HM, 6940-17, 6940-17-00-HM, 6940-17-TB-HM, 6940-19-TB-HM, 6940-26-TB, 6940-26-TB-HM, 6940-27-TB-HM, 69402N, 69402NT, 6940-30, 6940-32, 6940-32-TB, 6940-33-TB-HM, 69403N, 69403NH, 69403NT, 69403NW, 6940-41-TB-HM, 69404N, 69404NDH, 69404NH, 69404NHT, 69404NT, 69404NWT, 6940-60-TB-HT, 6940-62, 6940-62-TB, 6940-62-TB-HM, 6940-62-TB-HT, 6940-63-TB, 69406N, 69406NH, 69407N , 69407NT, 69414N, 69414NH, 69414NT, 69415N, 69415NH, 69415NHT, 69416N, 69416NHT, 69416NT, 69417N, 69417NHT, 69417NT, 69417NW, 69419NHT, 69427NHT, 69429NT, 69430NH, 69432N, 69432NT, 69433N, 69433NH, 69433NHT, 69433NT, 69434N, 69434NHT, 69437NH, 69437NHT, 69441NHT, 69444ND, 69444NDH, 69460N, 69460NHT, 69460NWT, 69461NH, 69462N, 69462NHT, 69462NT, 69463N, 69463NH, 69463NT, 69463NWT, 69466NWT, 69467N, 6950-03, 6950-03-00-HT, 6950-04-00-HM, 6950-04-TB-HT, 6950-06-TB-HM, 6950-15, 6950-16-TB-HM, 6950-19-TB-HM, 6950-19-TB-HT, 6950-26-TB-HM, 6950-27-TB-HM, 69502NH, 6950-33, 6950-33-TB-HM, 6950-39-00-HM, 69503N, 69503N, 69503NH, 69503NT, 6950-41-00-HT, 69504N, 69504NH, 69504NW, 6950-60, 6950-60-TB-HT, 6950-62-00-00-PB, 6950-62-TB-HT, 69506NHT, 69514N, 69514NH, 69514NHT, 69514NT, 69515N, 69515NH, 69516N, 69516NHT, 69516NT, 69517N, 69517NH, 69517NHT, 69517NT, 69519NHT, 69527NHT, 69529NT, 69530NH, 69532N, 69532NT, 69533N, 69533NH, 69533NHT, 69534N, 69541NHT, 69544ND, 69560N, 69560NHT, 69560NWT, 69561N, 69561NH, 69562N, 69562NHT, 69563NH, 69563NWT.

Product code INM

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)