medical MODERATE Updated 2026-07-08

Boston Scientific Corporation recalls CRE Wireguided 6-8mm 240cm

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Recalled Product

CRE Wireguided 6-8mm 240cm

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Hazard / Issue

Potential sterile breach of the pouches in which devices are packaged.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UPN: M00558450; GTIN: 8714729339380; Lot No. 38064056, 38064057, 38200574, 38200575, 38204501, 38204504, 38204506, 38204508, 38628161, 38640993, 38767490, 38904960, 38904961, 38946757, 38946758, 38946759; Exp. October 27, 2028 February 24, 2029.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for CRE Wireguided 6-8mm 240cm →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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