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Home > Recalled Products > Medical Devices > Defect > STAT-Check, Medline Resuscitator Bags

Recall: STAT-Check, Medline Resuscitator Bags

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On 2018-06-01, the FDA announced that SunMed Holdings is conducting a recall on Resuscitator Bags due to a possible defect. The recalled products were sold under the brand name(s) STAT-Check and Medline during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 1 medical devices recalls due to potential defect, including infant/child reduced energy defibrillation electrodes, catheters and more. Additionally, there have been 3 drug and medical device recalls due to other health hazards as well as 100 food recalls.

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SunMed Holdings, LLC , Logo
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Company Contact Information:

Name: SunMed Holdings
Website: www.sun-med.com
Phone: 1-800-433-2797

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Detailed Recall Information



Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.

Product Description: Resuscitator Bags

Brand Name(s): STAT-Check, Medline

Reason for Recall: Defect

Official Recall Date: 2018-06-01


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Additional information provided by the FDA.gov:

SunMed Holdings, LLC Issues a Nationwide Recall of STAT-Check and Medline Manual Resuscitator Bags

For Immediate Release
June 1, 2018

Contact
Consumers

info@sun-med.com 1-800-433-2797

Announcement

On May 29, 2018, SunMed Holdings, LLC initiated a nationwide recall of 18,808 units of STAT-Check and Medline resuscitator bags which were distributed between February 1, 2018 to May 13, 2018. The patient port retaining ring of the affected bags may not fully seat which may allow the patient port to detach during use. If this takes place, the resuscitator bags may not deliver air to the patient and result in a delay in treatment and life-threatening health consequences. There have been no reported injuries to date.

End users who have STAT-Check or Medline resuscitator bags within the lot numbers listed below should stop using them and immediately contact SunMed Holdings, LLC for further instructions on the return of these products.

The list below provides the resuscitator bag series, features, and respective lot numbers of the recalled models:

STAT-Check MANUAL RESUSCITATOR I VENTILATOR, REF SC9200MBP-1; Lot Numbers: 313406, 313447, 313164, 313165 & 313166

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR AND 7 FT. OXYGEN TUBING, REF CPRM1116; Lot Numbers:313298,313516,313588,313589, 313058,313060,313125,313173,313297, 313714, 313715 & 313774

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, FILTER AND 7 FT. OXYGEN TUBING, REF CPRM1116F; Lot Number: 313238

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, FILTER, C02 AND 7 FT. OXYGEN TUBING, REF CPRM1116FC; Lot Numbers: 313444 & 313239

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1116P; Lot Number: 313545

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, PEEP VALVE, C02 AND 7 FT. OXYGEN TUBING, REF CPRM1116PC; Lot Number: 313235

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK 5, BAG RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1116PD5; Lot Numbers: 313326, 313436 & 313049

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR AND 7 FT. OXYGEN TUBING, REF CPRM1126; Lot Numbers: 313546, 313717, 313176 & 313772

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, C02 AND 7 FT. OXYGEN TUBING, REF CPRM1126C; Lot Numbers: 313321, 313437, 313080 & 313193

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER AND 7 FT. OXYGEN TUBING, REF CPRM1126F; Lot Numbers: 313471, 313627 & 313696

MEDLINE ADULT MANUAL RESUSCITATOR WITH LARGE ADULT MASK, TUBE RESERVOIR, FILTER AND 7 FT. OXYGEN TUBING, REF CPRM1126FL; Lot Numbers: 313363 & 313738

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1126FP; Lot Numbers: 313323, 313355, 313739, 313031, 313093, 313190 & 313272

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE, C02 AND 7 FT. OXYGEN TUBING, REF CPRM1126FPC; Lot Number: 313315

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1126P; Lot Numbers: 313502 & 313741

The recalled products were distributed nationwide and can be identified by the part number, description, and lot number on the case labels, as well as a label on the individual packaging bag.

SunMed Holdings, LLC notified its distributors and these distributors have notified their customers by a direct mailing and will arrange for the return and replacement of all recalled resuscitator bags listed above.

End Users with questions may contact SunMed Holdings, LLC via telephone at 1-800-433-2797 between the hours of 8:30 AM to 5:00 PM (EST) Monday through Friday. End Users may also contact SunMed Holdings, LLC via e-mail at info@sun-med.com.

Adverse events or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting Program either online, by regular mail or by fax.

Complete and submit the report Online: www.fda.gov/medwatch/report.htm Regular Mail or Fax: download form www.fda.gov/MedWatch/getforms.htm or call 1-800-FDA-1088 to request form, then complete and return address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.


More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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