medical LOW RISK Updated 2026-03-18

Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010

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Recalled Product

Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB

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Hazard / Issue

The device does not bear a unique device identifier.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 0085007365401; Serial Numbers: 12193105601 09246762101 09246762102 07203174301 07205587001 12236633201 12236633202 09216175802 09216175801 05226320101 05216099201 05216099202 10216200701 01203114101 10193088201 10193088202 05205560701 05205559901 07216148001 07216148002 02226267201 02226267202 06246721701 06246721702 05236523001 05236523002 05236523003 03216064601 03216064602 09185135701 09185135702 11246790502 11246790501 04236501905 04236501902 04236501901 04236501904 07226354201 01236448201 01236448202 01236448203 01236448204 01236448205 01236448206 01236448207 01236448208 08142214601 08236570201 05226328502 05226328501 05226328504 05226328505 11195429001 11195429101 09246761301 09246761302 08185103701 01226253101 08195355001 09205628901 09205629001 08246753101 08246753104 08246753105 08246753106 08246753102 08246753103 02236477101 10182928001 10185152601 10236608401 10236608402 09195378101 09195378001 09195378301 09195378201 11195442101 11195442201 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02205499601 09205631501 09205631601 05216102601 06216120601 01226249601 04195281001 04195281101 01256821601 01256821602 04236503601 04236503602 04226311501 04226311502 12236630701 12236630702 07246742101 04246689802 03226286001 03226286002 03226286003 03226286004 10246788801 10246788802 03040570501 08195369001 08195369101 11226431101 11226431102 11226431103 11226431104 11226431105 11226431106 06246720301 10193078501 11193091301 03192999001 03226289802 03226289801 11195423001 02195222201 04195277701 02195222302 06195320201 01246656901 01246656902 01226252301 01226252302 04226310001 04226310002 04226310003 04226310004 04226310005 04226310006 09226395103 09226395104 09226395102 09226395101 08246758701 08246758702 08236566001 08236566002 06236541703 06236541702 06236541704 06236541701 05246709101 05246709102 08236573801 08236573802 08236573803 08236573804 08236573701 08236573702 08236573703 01192956501 01256823302 01256823307 01256823301 01256823304 01256823305 12246806101 01226253401 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✅ 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?

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View official government recall

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