FDA Device Intelligence
Home › Haslam Medical, Inc. › Motion Medical Distributing

Motion Medical Distributing

Haslam Medical, Inc. · Model 1703 · UDI-DI 15060498450239

OKV
0
510(k) clearances
30
Adverse events
94
Recalls
26
Facilities

Description

#1703 Obstetrical Kit Contents: (2) Gloves L/F, (1) Underpad 17x24", (2) Umbilical Clamps, (2) Obstetrical Towelettes, (1) Scalpel #22, (1) Obstetrical Pad, (1) Receiving Blanket, (3) Sponge 4x4 2/Pk, (1) Bulb Syringe, (4) Towels 3-Ply, (2) Nylon Ties, (2) Alcohol Prep Pad, (3) Twist Ties, (1) Biohazard bag, (1) Placenta Bag

Recalls

DateFirmReason
2026-08-10AVID Medical, Inc.Product may be potentially contaminated with a lubricant used during the manufacturing process.
2026-08-10AVID Medical, Inc.Product may be potentially contaminated with a lubricant used during the manufacturing process.
2026-08-10AVID Medical, Inc.Product may be potentially contaminated with a lubricant used during the manufacturing process.
2026-07-10Medline Industries, LPKits contain a potentially contaminated component which were recalled by the manufacturer
2026-07-10AVID Medical, Inc.A customer complaint reported that the Clearify Visualization System (5303907) leaked in a kit. As a result of Avid s investigation, it was determined that the component was subjec
2026-06-08Medline Industries, LPAffected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter
2026-05-04Medline Industries, LPDuring an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac
2026-04-27Medline Industries, LPKits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
2026-03-19Medline Industries, LPDuring an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o
2026-02-25Medline Industries, LPThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.