Reported Dec 21, 2022 · Ongoing
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Stryker Medical Division of Stryker Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Medical Division of Stryker Corporation · 3800 E Centre Ave · Portage, MI · 49002-5826
Is this the product you have?
Power-PRO 2Model No. 6507Item No. 650705550001 (US)650700000000 (International)
- Lot codes and dates
- UDI-DI (GTIN) 07613327504460 Serial Numbers
374 of 374 codes
220400034322040003452204000348220400035122040003692204000370220400038222040004302204000673220400068222050000942205000095220500009622050000972205000098220500009922050001002205000101220500010222050001042205000105220500010922050001102205000111220500011322050001152205000117220500011922050001232205000124220500012522050001282205000129220500013022050001322205000135220500013722050001392205000142220500014322050001512205000170220800165822080016602203001748220400043122040006512204000663220400066522040006672204000670220400067122040006802203001948220300195522040000752204000094220400009722040006322204000633
- UDI-DI (GTIN) 07613327504460 Serial Numbers
- Amount recalled
- 465 (403 US; 62 OUS)
Where it was sold
- Nationwide
Why it was recalled
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
This product could cause temporary or reversible health problems — stop using it.
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