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RecallWatchMedical Device Safety
Class IIOngoingZ-1580-2026

Stryker Medical Division Of Stryker Corporation recalls Cub Pediatric Crib

Stryker Medical Division of Stryker CorporationPortage, MI, United StatesReported Mar 25, 2026 · 3 months ago
Legal News Analyst ·

Reason for recall

Cribs sold in the USA are missing two access door warning labels.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Cub Pediatric Crib, ModelFL19H
    400 affected lots
    F61948F61875F61710F62449F62450F62451F62452F62047
    +392 moreF62048F62498F62499F62500F61619F61620F61621F61622F61623F61624F61625F61626F61627F61628F61629F61630F61631F61632F61633F61634F61635F61636F61637F61638F61639F61640F61641F61642F61643F61644F61645F61646F61647F61648F61649F61650F61651F61652F61653F61654F61655F61656F61657F61658F61659F61660F61661F61662F61663F61664F61665F61666F61667F61668F61669F61670F61671F61672F61673F61674F61675F61676F61677F61678F61679F61680F61681F61682F61683F61684F61685F61686F61687F61688F61889F61890F61891F61892F61893F61698F61699F62448F61972F61988F61989F62181F62501F62502F62532F62533F62432F62446F62447F61595F61992F61993F62125F62389F61894F62123F61742F61743F62117F62118F62119F62433F62434F62435F62436F62437F61917F61918F61919F61920F61921F61922F61923F61924F61925F61926F61927F61928F61929F61930F61865F61866F62159F62160F62161F62325F62158F62204F62205F62524F62525F61695F61696F61729F62083F62084F62085F62086F62087F61763F61764F61765F61766F61767F61768F61769F61770F61771F61772F62431F62394F62395F62396F62397F62398F62399F62400F62401F62402F62403F62419F62420F62421F62422F62423F62424F62425F61998F61693F61694F62530F62531F61697F61700F62371F62372F62373F62374F62375F62195F62015F62248F62249F62380F61945F61946F61947F62146F62147F62331F62332F62333F62334F61933F61934F61935F61936F61937F61938F61939F61940F61941F61942F61943F61944F61575F61576F61577F61604F61605F61606F61607F61608F61609F61611F61612F61613F61614F62010F62011F62012F62013F62014F61910F61911F61912F61785F62044F62045F61991F62462F61826F61827F61828F61829F61830F61831F61832F61833F61834F61835F61836F61837F62116F62246F62247F62459F62460F62518F62519F61741F61745F61746F62177F62178F62179F62180F62453F62454F61915F61916F62552F62553F62554F62555F62556F62557F62558F62559F62126F62335F62336F62337F62338F62339F62340F62341F62342F62343F62344F62345F62346F62347F62348F62349F62350F62351F62352F62353F62354F62355F61570F61970F62503F62504F62505F62506F62507F62508F62509F62510F62511F62512F62513F62514F62515F62516F62517F62305F62429F62430F62303F62304F62370F61788F61789F61790F61791F61792F61793F61794F61795F61796F61797F62226F62227F61881F61882F61883F61884F61885F61886F61887F61888F62077F61711F61712F61713F61714F62382F62388F61717F61718F61719F61720F61721F61736F61737F61738F61739F61740F62033F61701F61702F61703F61704F61705F61857F61858F61786F61787F62306F62307F62356F62357F62358F62359F62360F62361F61581F61715F61716F62148F62149F62150F62151F62152F62153F61838F61839F61840F61841F61842F61843F61913F61914F62108F62109

What the firm is doing

On February 18. 2026, the firm notified customers through IMPORTANT MEDICAL DEVICE CORRECTION letters. Customers were notified of the missing warning labels, which read, "WARNING: Never leave a child unsupervised when the movable slide is open or not secured Refer to Instructions for Use for product care, maintenance, and cleaning." Customers were instructed to locate the units listed on the attached business reply form and identify the address where they can be serviced, and return the completed form to Stryker. Stryker will then contact consignees to arrange for the application of the missing label. In the interim, until the service can be performed, all pertinent warnings and safety instructions may be found in the product manual: https://techweb.stryker.com/Stretcher/FL19/1607/Operations/1900-109- 001AC.0.pdf

DistributionShow details

US Nationwide distribution.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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