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Recall Observatory FDA recall evidence

Device product

Medline Convenience kits used for various procedures: 1) DENTAL PACK-LF, Model Number: DYNJ84880; 2) DENTAL PACK, Model Number: DYNJ56229A; 3) DENTAL PACK-LF, Model Number: PHS807626F; 4) DENTAL PACK SMGH, Model Number: DYNJ41929D; 5) DENTAL PACK, Model Number: DYNJ51841C; 6) NYGH-MINOR DENTAL-PLASTIC-LF, Model Number: DYNJ905551C

Z-1595-2025

March 03, 2025

Class II

Product summary

Firm
MEDLINE INDUSTRIES, LP - Northfield
Event
Event 96510
Status
Ongoing
Classification
Class II
Quantity
573 units
Official record key
device-enforcement:Z-1595-2025

Official wording

Reason: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Code information: 1) DYNJ84880, UDI-DI: 10195327432140(each), 40195327432141(case), Lot Number: 24JBL926; 2) DYNJ56229A, UDI-DI: 10198459108105(each), 40198459108106(case), Lot Number: 24JBV124; 3) PHS807626F, UDI-DI: 10198459028045(each), 40198459028046(case), Lot Number: 24JBV611; 4) DYNJ41929D, UDI-DI: 10198459160585(each), 40198459160586(case), Lot Number: 24JBW877; 5) DYNJ51841C, UDI-DI: 10195327522186(each), 40195327522187(case), Lot Number: 24KBA623; 6) DYNJ905551C, UDI-DI: 10195327556099(each), 40195327556090(case), Lot Number: 24KBN091

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.