Reported Jul 1, 2015 · Terminated
Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual…
Teleflex Medical
High riskUsing this product could cause serious injury, illness or death — stop using it now.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: Teleflex Medical · 2917 Weck Dr · Research Triangle Park, NC · 27709-0186
Is this the product you have?
- Lifesaver Single Patient
- Use Manual Resuscitator Product UsageThe Hudson RCI Lifesaver Single Patient Use manual resuscitator with pressure monitoring port is a disposable medical device intended for use on patients requiring temporary augmentation of ventilation with or without supplemental oxygen delivery during episodes of acute ventilatory failure or insufficiency
- Lot codes and dates
84 of 84 products
Products covered by this recall Model / number Product as published — Lot No. 140514 - 4 Digit — Lot No. 1420; 6 Digit — Lot No. 140616 4 Digit — Lot No. 1425, 6 Digit — Lot No. 140617 4 Digit — Lot No. 1425; 6 Digit — Lot No. 140621 4 Digit — Lot No. 1425; 6 Digit — Lot No. 140806 4 Digit — Lot No. 1432; 6 Digit — Lot No. 141103 4 Digit — Lot No. 1445; 6 Digit — Lot 141117 - No. 4 Digit — Lot No. 1447; 6 Digit — Lot No. 141201- 4 Digit — Lot No. 1449; 6 Digit — Lot No. 141224 - 4 Digit — Lot No. 1452; 6 Digit — Lot No. 141227 - 4 Digit — Lot No. 1452; 6 Digit - Amount recalled
- 9,333 units
Where it was sold
Why it was recalled
Stop using this product now
The intake port may be blocked which can cause the bag to fail to fill.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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