IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20... — FDA record Z-2462-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 12, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20171963, h) B20171973, i) B20172253, j) B20172263, k) B20172273; intervertebral fusion device - cervical
Reason
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Classification
Class II
Recalling firm
Medicrea International
Quantity
N/A
Agency-reported status
Ongoing
Source record identifier
Z-2462-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilitya) B20171743, GTIN 03613720232636, Lot Numbers: 18E0275, 18E0404, 18E0676, 18E0833, 18I0867, 18K0143, 18L0219, 19A0463, 19A0669, 19B0870, 19D0484, 19G0192, 19G0422, 19J0468, 19L0381, 20F0631, 20G0849, 20H0596, 20H0597, 20H0598, 20I0875, 20J0772, 21I0163, 22A0172, 22D0807, 22E0264, 22G0048, 22G0477, 22I0342; b) B20171753, GTIN 03613720232667, Lot Numbers: 18H0597, 18K0137, 18K0831, 18L0488, 19A0324, 19A0325, 19B0362, 19B0470, 19D0485, 19E0322, 19G0204, 19G0423, 19I0274, 19J0273, 19L0382, 20F0632, 20F0633, 20H0600, 20H0601, 20H0602, 20H0603, 20I0222, 21C0104, 21F0651, 21I0511, 22I0615, 22J0265; c) B20171763, GTIN 03613720232698, Lot Numbers: 18E0405, 18E0834, 18G0422, 18H0572, 18J0063, 18K0066, 18L0070, 18L0489, 19A0215, 19A0425, 19B0687, 19C0653, 19D0486, 19E0436, 19G0830, 19I0842, 19L0383, 20F0634, 20H0594, 20H0595, 21E0234, 21G0482, 22I0343; d) B20171773, GTIN 03613720232728, Lot Numbers: 19C0591, 19F0579, 19H0089, 19J0272, 20F0635, 20H0249, 22G0571; e) B20171943, GTIN 03613720232841, Lot Numbers: 18C0552, 18E0835, 18I0712, 18K0897, 18L0490, 19A0670, 19B0680, 19D0251, 19G0302, 19I0582, 20A0644, 20F0636, 20H0599, 20I0487, 21H0101, 22A0173, 22B0482, 22D0808, 22E0808; f) B20171953, GTIN 03613720232872, Lot Numbers: 18E0483, 18E0677, 18E0836, 18J0103, 18K0144, 18L0400, 19A0159, 19A0671, 19A0675, 19B0089, 19D0487, 19D0637, 19F0103, 19G0303, 19H0375, 19I0843, 19K0586, 20A0200, 20C0163, 20F0637, 20H0251, 20H0254, 20H0255, 20J0062, 20J0065, 20J0368, 21F0551, 21I0177, 22B0786, 22E0263, 22E0809, 22F0490, 22F0492, 22G0440, 22H0055, 22J0202; g) B20171963, GTIN 03613720232902, Lot Numbers: 18K0158, 18L0491, 19A0672, 19A0829, 19C0146, 19D0262, 19E0437, 19G0424, 19H0376, 19I0234, 19K0832, 19L0613, 20A0969, 20F0638, 20H0604, 20H0605, 20H0606, 20H0607, 20I0705, 20J0068, 21F0155, 22D0809, 22G0441, 22H0643, 22J0203,; h) B20171973, GTIN 03613720232933, Lot Numbers: 18D0171, 18F0203, 18I0466, 18K0136, 18L0492, 19A0673, 19D0488, 19I0844, 20H0257, 21A0064, 22D0385, 22F1090, 22G0442; i) B20172253, GTIN 03613720233084, Lot Numbers: 18E0406, 18K0140, 18K0898, 19A0214, 19B0174, 19C0728, 19E0438, 19I0583, 20H0258, 20K0542, 21G0760; j) B20172263, GTIN 03613720233114, Lot Numbers: 18D1078, 18G0423, 18K0159, 18L0220, 19A0069, 19B0175, 19E0439, 19I0845, 20A0995, 20F0386, 20H0593, 20J0127, 21F0247, 21J0503; k) B20172273, GTIN 03613720233145, Lot Numbers: 18K0160, 18K0608, 19A0079, 19B0471, 19C0729, 19D0671, 19J0469, 20H0259, 22B0180, 22B0484, 22E0095

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US nationwide

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Aug 30, 2023
Recall initiation date
Jul 12, 2023
Center classification date
Aug 24, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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