Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-235; Color Cuff Single Port, Single Bladder 34 (Purple), Quick Connect, REF: 5921-034-135; Color Cuff Dual Port, Single Bladder 34 (Purple), Quick Connect, REF: 5921-034-235; Color Cuff Single Port, Single Bladder 18 (Red), Quick Connect, REF: 5921-218-135; Color Cuff Dual Port, Single Bladder 18 (Red), Quick Connect, REF: 5921-218-235;
Class I - DangerousWhat Should You Do?
- Check if you have this product: REF/UI-DI: 5921-030-135/885825016142, 5921-030-235/885825016166, 5921-034-135/885825016173, 5921-034-235/885825016197, 5921-218-135/885825016500, 5921-218-235/885825016296 Lots: 0000202775, 0000209215, 0000202137, 0000201380, 0000200708, 13872322, 13453772, 0000198235, 0000202066, 0000209420, 0000206425, 0000192978, 0000202577, 0000192465, 13463347, 0000204578, 0000193181, 0000198446, 0000208949, 0000195337, 0000206263, 0000193179, 13486613, 0000202777, 0000195071, 0000204159, 0000195912, 0000200905, 0000206442, 0000197869, 13594486, 0000192979, 0000200706, 0000195068, 0000201379, 0000199502, 0000199434, 0000188863, 13493683, 0000193177, 0000202065, 0000200712, 0000200242, 0000202138, 13582864, 0000195075, 13570832, 0000199808, 0000202075, 0000195340, 0000200254, 0000202932, 13774680, 13851472, 13634704, 0000199819, 0000204319, 0000204160, 0000201378, 0000200227, 0000203311, 0000206583, 13235119, 0000194243, 0000196364, 0000193841, 0000200270, 13828088, 0000196363, 13392486, 13280380, 0000192981, 0000198461, 0000196361, 0000200244, 0000203310, 0000200229, 13398036, 13352572, 0000194232, 0000200253, 0000198245, 0000202776, 0000197373, 0000187746, 13765829, 13449838, 0000200256, 0000202145, 0000198246, 0000198236, 0000204574, 0000202143, 0000194242, 13583025, 0000202074, 0000203315, 0000195073, 0000193176, 0000212764, 0000196379, 13811283, 13605685, 0000187310, 0000208444, 0000204366, 0000197867, 13865381, 13820702, 0000176566, 13663274, 0000196365, 0000210787, 0000206440, 0000193391, 0000201391, 0000193412, 0000177131, 13883084, 0000198460, 0000208345, 0000206443, 0000192466, 0000210962, 0000200230, 0000204570, 13339407, 0000204314, 0000211530, 0000209200, 0000196359, 0000210005, 0000201840, 0000205922, 0000192980, 0000205238, 0000195335, 0000206518, 0000195067, 0000203313, 0000193393, 0000206254, 0000208440, 0000202686, 0000198244, 0000203314, 0000195069, 0000208407, 0000206432, 13632837, 0000210465, 0000206505, 0000172873, 0000195338, 0000199805, 0000208321, 0000195343, 0000205241, 0000200707, 0000199807, 0000195076, 0000197375, 0000203312, 13870728, 0000202139, 0000206511, 0000193392, 13824462, 0000195070, 0000199816, 0000208410, 13871893, 0000199503, 0000206586, 13272167, 13399919, 0000195072, 0000199817, 0000192977, 0000197872, 0000186596, 0000208322, 13573489, 0000209992, 0000202684, 0000211154, 0000201837, 0000210310, 0000197870, 0000208606, 0000204571, 13883045, 0000197376, 0000194228, 0000204195, 0000198237, 0000212878, 0000209416, 0000210963, 0000210601, 0000200711, 0000194229, 0000204372, 0000196362, 13807840, 0000210008, 0000200228, 0000172314, 0000200257, 0000194230, 0000205930, 0000193839, 0000193178, 0000210313, 0000198459, 13814050, 0000202144, 0000193413, 0000195336, 13765599, 0000208951, 0000195078, 0000194227, 0000193838, 0000193840, 0000202778
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Stryker Sustainability Solutions
- Reason for Recall:
- Increased incidence of disposable tourniquet cuffs "not able to achieve desired pressure" and "not holding pressure" due to 1) Cuff fabric tearing during use, and 2) Pinched or unseated O-ring at the connection between the cuff, disposable fill line, and/or cuff hosing, which may lead to loss of vascular occlusion, which may lead to operative site blood loss, hemorrhage, or other complications.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-235; Color Cuff Single Port, Single Bladder 34 (Purple), Quick Connect, REF: 5921-034-135; Color Cuff Dual Port, Single Bladder 34 (Purple), Quick Connect, REF: 5921-034-235; Color Cuff Single Port, Single Bladder 18 (Red), Quick Connect, REF: 5921-218-135; Color Cuff Dual Port, Single Bladder 18 (Red), Quick Connect, REF: 5921-218-235;
Product Codes/Lot Numbers:
REF/UI-DI: 5921-030-135/885825016142, 5921-030-235/885825016166, 5921-034-135/885825016173, 5921-034-235/885825016197, 5921-218-135/885825016500, 5921-218-235/885825016296 Lots: 0000202775, 0000209215, 0000202137, 0000201380, 0000200708, 13872322, 13453772, 0000198235, 0000202066, 0000209420, 0000206425, 0000192978, 0000202577, 0000192465, 13463347, 0000204578, 0000193181, 0000198446, 0000208949, 0000195337, 0000206263, 0000193179, 13486613, 0000202777, 0000195071, 0000204159, 0000195912, 0000200905, 0000206442, 0000197869, 13594486, 0000192979, 0000200706, 0000195068, 0000201379, 0000199502, 0000199434, 0000188863, 13493683, 0000193177, 0000202065, 0000200712, 0000200242, 0000202138, 13582864, 0000195075, 13570832, 0000199808, 0000202075, 0000195340, 0000200254, 0000202932, 13774680, 13851472, 13634704, 0000199819, 0000204319, 0000204160, 0000201378, 0000200227, 0000203311, 0000206583, 13235119, 0000194243, 0000196364, 0000193841, 0000200270, 13828088, 0000196363, 13392486, 13280380, 0000192981, 0000198461, 0000196361, 0000200244, 0000203310, 0000200229, 13398036, 13352572, 0000194232, 0000200253, 0000198245, 0000202776, 0000197373, 0000187746, 13765829, 13449838, 0000200256, 0000202145, 0000198246, 0000198236, 0000204574, 0000202143, 0000194242, 13583025, 0000202074, 0000203315, 0000195073, 0000193176, 0000212764, 0000196379, 13811283, 13605685, 0000187310, 0000208444, 0000204366, 0000197867, 13865381, 13820702, 0000176566, 13663274, 0000196365, 0000210787, 0000206440, 0000193391, 0000201391, 0000193412, 0000177131, 13883084, 0000198460, 0000208345, 0000206443, 0000192466, 0000210962, 0000200230, 0000204570, 13339407, 0000204314, 0000211530, 0000209200, 0000196359, 0000210005, 0000201840, 0000205922, 0000192980, 0000205238, 0000195335, 0000206518, 0000195067, 0000203313, 0000193393, 0000206254, 0000208440, 0000202686, 0000198244, 0000203314, 0000195069, 0000208407, 0000206432, 13632837, 0000210465, 0000206505, 0000172873, 0000195338, 0000199805, 0000208321, 0000195343, 0000205241, 0000200707, 0000199807, 0000195076, 0000197375, 0000203312, 13870728, 0000202139, 0000206511, 0000193392, 13824462, 0000195070, 0000199816, 0000208410, 13871893, 0000199503, 0000206586, 13272167, 13399919, 0000195072, 0000199817, 0000192977, 0000197872, 0000186596, 0000208322, 13573489, 0000209992, 0000202684, 0000211154, 0000201837, 0000210310, 0000197870, 0000208606, 0000204571, 13883045, 0000197376, 0000194228, 0000204195, 0000198237, 0000212878, 0000209416, 0000210963, 0000210601, 0000200711, 0000194229, 0000204372, 0000196362, 13807840, 0000210008, 0000200228, 0000172314, 0000200257, 0000194230, 0000205930, 0000193839, 0000193178, 0000210313, 0000198459, 13814050, 0000202144, 0000193413, 0000195336, 13765599, 0000208951, 0000195078, 0000194227, 0000193838, 0000193840, 0000202778
Distribution:
Nationwide distribution
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1315-2023
Related Recalls
HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
Stryker Sustainability Solutions
Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.
Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A
Stryker Sustainability Solutions
Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Stryker Sustainability Solutions
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.